Canonical Allele Identifier: CA2036978826
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429925C= , CM000674.2:g.53429925C= GRCh38
NC_000012.11:g.53823709C= , CM000674.1:g.53823709C= GRCh37
NC_000012.10:g.52109976C= NCBI36
NG_015981.1:g.11071C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1235C= MANE Select ENSP00000257863.3:p.Ser412=
ENST00000257863.8:c.1235C= ENSP00000257863.3:p.Ser412=
ENST00000379791.7:c.1140+300C= ENSP00000369117.3:n.1140+300C=
ENST00000550311.5:c.1235C= ENSP00000446661.1:p.Ser412=
ENST00000550839.1:c.326C= ENSP00000455338.1:p.Ser109=
ENST00000552233.5:n.823C=
NM_001164690.1:c.1235C= NP_001158162.1:p.Ser412=
NM_001164691.1:c.1140+300C= NP_001158163.1:n.1140+300C=
NM_020547.2:c.1235C= NP_065434.1:p.Ser412=
XM_011538173.1:c.1295C= XP_011536475.1:p.Ser432=
XM_011538174.1:c.1292C= XP_011536476.1:p.Ser431=
XM_011538175.1:c.1277C= XP_011536477.1:p.Ser426=
XM_011538176.1:c.1238C= XP_011536478.1:p.Ser413=
XM_011538177.1:c.1217C= XP_011536479.1:p.Ser406=
XM_011538178.1:c.1076C= XP_011536480.1:p.Ser359=
XM_011538179.1:c.1200+300C= XP_011536481.1:n.1200+300C=
XM_011538180.1:c.962C= XP_011536482.1:p.Ser321=
XM_011538181.1:c.959C= XP_011536483.1:p.Ser320=
XM_011538182.1:c.884C= XP_011536484.1:p.Ser295=
XM_011538183.1:c.1201-221C= XP_011536485.1:n.1201-221C=
XM_011538184.1:c.1220+280C= XP_011536486.1:n.1220+280C=
XM_011538185.1:c.856-1252C= XP_011536487.1:n.856-1252C=
XM_011538186.1:c.410C= XP_011536488.1:p.Ser137=
NM_001164690.2:c.1235C= NP_001158162.1:p.Ser412=
NM_001164691.2:c.1140+300C= NP_001158163.1:n.1140+300C=
NM_020547.3:c.1235C= MANE Select NP_065434.1:p.Ser412=
XM_011538183.2:c.1201-221C= XP_011536485.1:n.1201-221C=
XM_011538184.2:c.1220+280C= XP_011536486.1:n.1220+280C=
XM_011538186.3:c.410C= XP_011536488.1:p.Ser137=
XM_017019179.2:c.1295C= XP_016874668.1:p.Ser432=
XM_024448938.1:c.1143+300C= XP_024304706.1:n.1143+300C=
XR_002957309.1:n.1203C=
XR_002957310.1:n.1109-221C=
XR_002957311.1:n.1203C=
XR_002957312.1:n.1108+300C=