Canonical Allele Identifier: CA12960672
Gene: NTRK2 HGNC NCBI

Linked Data

dbSNP Id: rs1122530
gnomAD v2: 9-87464352-A-G
gnomAD v3: 9-84849437-A-G
gnomAD v4: 9-84849437-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.84849437A>G , CM000671.2:g.84849437A>G GRCh38
NC_000009.11:g.87464352A>G , CM000671.1:g.87464352A>G GRCh37
NC_000009.10:g.86654172A>G NCBI36
NG_012201.2:g.185887A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000304053.11:c.1397-17806A>G ENSP00000306167.7:n.1397-17806A>G
ENST00000323115.11:c.1361-17806A>G ENSP00000314586.5:n.1361-17806A>G
ENST00000685095.1:n.2062-17806A>G
ENST00000685463.1:n.2062-17806A>G
ENST00000685720.1:c.1397-11603A>G ENSP00000509031.1:n.1397-11603A>G
ENST00000686259.1:c.1397-17806A>G ENSP00000509743.1:n.1397-17806A>G
ENST00000686324.1:c.1397-11603A>G ENSP00000510134.1:n.1397-11603A>G
ENST00000686332.1:n.2475-17806A>G
ENST00000686443.1:c.1397-17806A>G ENSP00000509093.1:n.1397-17806A>G
ENST00000686496.1:c.1397-17806A>G ENSP00000510060.1:n.1397-17806A>G
ENST00000687386.1:c.1397-17806A>G ENSP00000508723.1:n.1397-17806A>G
ENST00000687636.1:c.1397-11603A>G ENSP00000508829.1:n.1397-11603A>G
ENST00000688333.1:n.2330-17806A>G
ENST00000689301.1:c.929-17806A>G ENSP00000510766.1:n.929-17806A>G
ENST00000690882.1:n.2062-17806A>G
ENST00000691788.1:c.1397-17806A>G ENSP00000509401.1:n.1397-17806A>G
ENST00000692181.1:c.1397-17806A>G ENSP00000510619.1:n.1397-17806A>G
ENST00000692473.1:c.929-11603A>G ENSP00000509020.1:n.929-11603A>G
ENST00000693539.1:c.1397-11603A>G ENSP00000510640.1:n.1397-11603A>G
ENST00000277120.8:c.1397-11603A>G MANE Select ENSP00000277120.3:n.1397-11603A>G
ENST00000323115.10:c.1397-17806A>G ENSP00000314586.4:n.1397-17806A>G
ENST00000376208.6:c.1397-17806A>G ENSP00000365381.1:n.1397-17806A>G
ENST00000376213.6:c.1397-17806A>G ENSP00000365386.1:n.1397-17806A>G
ENST00000277120.7:c.1397-11603A>G ENSP00000277120.3:n.1397-11603A>G
ENST00000304053.10:c.1397-11603A>G ENSP00000306167.6:n.1397-11603A>G
ENST00000323115.8:c.1397-17806A>G ENSP00000314586.4:n.1397-17806A>G
ENST00000376208.5:c.1397-17806A>G ENSP00000365381.1:n.1397-17806A>G
ENST00000376213.5:c.1397-17806A>G ENSP00000365386.1:n.1397-17806A>G
ENST00000376214.5:c.1397-11603A>G ENSP00000365387.1:n.1397-11603A>G
NM_001018064.2:c.1397-17806A>G NP_001018074.1:n.1397-17806A>G
NM_001018065.2:c.1397-11603A>G NP_001018075.1:n.1397-11603A>G
NM_001018066.2:c.1397-17806A>G NP_001018076.1:n.1397-17806A>G
NM_006180.4:c.1397-11603A>G NP_006171.2:n.1397-11603A>G
XM_005252001.1:c.1397-11603A>G XP_005252058.1:n.1397-11603A>G
XM_005252003.1:c.1397-11603A>G XP_005252060.1:n.1397-11603A>G
XM_005252004.1:c.1397-11603A>G XP_005252061.1:n.1397-11603A>G
XM_005252006.2:c.1397-11603A>G XP_005252063.1:n.1397-11603A>G
XM_011518718.1:c.1397-17806A>G XP_011517020.1:n.1397-17806A>G
XM_011518719.1:c.1397-17806A>G XP_011517021.1:n.1397-17806A>G
XM_011518720.1:c.1397-17806A>G XP_011517022.1:n.1397-17806A>G
XM_005252001.3:c.1397-11603A>G XP_005252058.1:n.1397-11603A>G
XM_005252003.3:c.1397-11603A>G XP_005252060.1:n.1397-11603A>G
XM_005252004.2:c.1397-11603A>G XP_005252061.1:n.1397-11603A>G
XM_005252006.4:c.1397-11603A>G XP_005252063.1:n.1397-11603A>G
XM_011518718.3:c.1397-17806A>G XP_011517020.1:n.1397-17806A>G
XM_011518720.3:c.1397-17806A>G XP_011517022.1:n.1397-17806A>G
XM_017014751.2:c.1397-11603A>G XP_016870240.1:n.1397-11603A>G
XM_017014752.1:c.1397-17806A>G XP_016870241.1:n.1397-17806A>G
XM_017014753.2:c.1397-17806A>G XP_016870242.1:n.1397-17806A>G
XM_017014754.1:c.1397-17806A>G XP_016870243.1:n.1397-17806A>G
XM_017014755.1:c.1397-11603A>G XP_016870244.1:n.1397-11603A>G
XM_017014756.1:c.1397-11603A>G XP_016870245.1:n.1397-11603A>G
XM_017014757.1:c.1397-17806A>G XP_016870246.1:n.1397-17806A>G
NM_001018064.3:c.1397-17806A>G NP_001018074.1:n.1397-17806A>G
NM_001018066.3:c.1397-17806A>G NP_001018076.1:n.1397-17806A>G
NM_001369532.1:c.1397-17806A>G NP_001356461.1:n.1397-17806A>G
NM_001369533.1:c.1397-17806A>G NP_001356462.1:n.1397-17806A>G
NM_001369534.1:c.1361-17806A>G NP_001356463.1:n.1361-17806A>G
NM_001369535.1:c.929-17806A>G NP_001356464.1:n.929-17806A>G
NM_001369536.1:c.929-11603A>G NP_001356465.1:n.929-11603A>G
NM_001369537.1:c.1397-11603A>G NP_001356466.1:n.1397-11603A>G
NM_001369538.1:c.1397-17806A>G NP_001356467.1:n.1397-17806A>G
NM_006180.5:c.1397-11603A>G NP_006171.2:n.1397-11603A>G
NM_006180.6:c.1397-11603A>G MANE Select NP_006171.2:n.1397-11603A>G