Canonical Allele Identifier: CA2036978844
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429949T= , CM000674.2:g.53429949T= GRCh38
NC_000012.11:g.53823733T= , CM000674.1:g.53823733T= GRCh37
NC_000012.10:g.52110000T= NCBI36
NG_015981.1:g.11095T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1259T= MANE Select ENSP00000257863.3:p.Ile420=
ENST00000257863.8:c.1259T= ENSP00000257863.3:p.Ile420=
ENST00000379791.7:c.1140+324T= ENSP00000369117.3:n.1140+324T=
ENST00000550311.5:c.1259T= ENSP00000446661.1:p.Ile420=
ENST00000550839.1:c.350T= ENSP00000455338.1:p.Ile117=
ENST00000552233.5:n.847T=
NM_001164690.1:c.1259T= NP_001158162.1:p.Ile420=
NM_001164691.1:c.1140+324T= NP_001158163.1:n.1140+324T=
NM_020547.2:c.1259T= NP_065434.1:p.Ile420=
XM_011538173.1:c.1319T= XP_011536475.1:p.Ile440=
XM_011538174.1:c.1316T= XP_011536476.1:p.Ile439=
XM_011538175.1:c.1301T= XP_011536477.1:p.Ile434=
XM_011538176.1:c.1262T= XP_011536478.1:p.Ile421=
XM_011538177.1:c.1241T= XP_011536479.1:p.Ile414=
XM_011538178.1:c.1100T= XP_011536480.1:p.Ile367=
XM_011538179.1:c.1200+324T= XP_011536481.1:n.1200+324T=
XM_011538180.1:c.986T= XP_011536482.1:p.Ile329=
XM_011538181.1:c.983T= XP_011536483.1:p.Ile328=
XM_011538182.1:c.908T= XP_011536484.1:p.Ile303=
XM_011538183.1:c.1201-197T= XP_011536485.1:n.1201-197T=
XM_011538184.1:c.1220+304T= XP_011536486.1:n.1220+304T=
XM_011538185.1:c.856-1228T= XP_011536487.1:n.856-1228T=
XM_011538186.1:c.434T= XP_011536488.1:p.Ile145=
NM_001164690.2:c.1259T= NP_001158162.1:p.Ile420=
NM_001164691.2:c.1140+324T= NP_001158163.1:n.1140+324T=
NM_020547.3:c.1259T= MANE Select NP_065434.1:p.Ile420=
XM_011538183.2:c.1201-197T= XP_011536485.1:n.1201-197T=
XM_011538184.2:c.1220+304T= XP_011536486.1:n.1220+304T=
XM_011538186.3:c.434T= XP_011536488.1:p.Ile145=
XM_017019179.2:c.1319T= XP_016874668.1:p.Ile440=
XM_024448938.1:c.1143+324T= XP_024304706.1:n.1143+324T=
XR_002957309.1:n.1227T=
XR_002957310.1:n.1109-197T=
XR_002957311.1:n.1227T=
XR_002957312.1:n.1108+324T=