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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.34489453G= , CM000671.2:g.34489453G=
GRCh38
NC_000009.11:g.34489451G= , CM000671.1:g.34489451G=
GRCh37
NC_000009.10:g.34479451G=
NCBI36
NG_008127.1:g.35641G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000242317.9:c.388+4G=
MANE Select
ENSP00000242317.4:n.388+4G=
ENST00000242317.8:c.388+4G=
ENSP00000242317.4:n.388+4G=
ENST00000437363.5:c.355+4G=
ENSP00000395396.1:n.355+4G=
ENST00000488369.1:n.504+4G=
ENST00000614641.4:c.388+4G=
ENSP00000480538.1:n.388+4G=
NM_001281428.1:c.388+4G=
NP_001268357.1:n.388+4G=
NM_012144.3:c.388+4G=
NP_036276.1:n.388+4G=
XM_011517846.1:c.388+4G=
XP_011516148.1:n.388+4G=
XM_011517847.1:c.388+4G=
XP_011516149.1:n.388+4G=
XM_011517848.1:c.388+4G=
XP_011516150.1:n.388+4G=
XM_011517849.1:c.388+4G=
XP_011516151.1:n.388+4G=
XM_011517850.1:c.388+4G=
XP_011516152.1:n.388+4G=
XR_929232.1:n.642+4G=
XR_929233.1:n.642+4G=
XR_929235.1:n.642+4G=
XM_006716758.3:c.-89+4G=
XP_006716821.1:n.-89+4G=
XM_011517846.2:c.388+4G=
XP_011516148.1:n.388+4G=
XM_011517847.3:c.388+4G=
XP_011516149.1:n.388+4G=
XM_011517848.2:c.388+4G=
XP_011516150.1:n.388+4G=
XM_011517849.2:c.388+4G=
XP_011516151.1:n.388+4G=
XM_011517850.3:c.388+4G=
XP_011516152.1:n.388+4G=
XM_017014625.2:c.388+4G=
XP_016870114.1:n.388+4G=
XR_002956774.1:n.589+4G=
XR_929232.2:n.589+4G=
XR_929233.2:n.589+4G=
NM_012144.4:c.388+4G=
MANE Select
NP_036276.1:n.388+4G=
NM_001281428.2:c.388+4G=
NP_001268357.1:n.388+4G=