Canonical Allele Identifier: CA2036978777
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429869C= , CM000674.2:g.53429869C= GRCh38
NC_000012.11:g.53823653C= , CM000674.1:g.53823653C= GRCh37
NC_000012.10:g.52109920C= NCBI36
NG_015981.1:g.11015C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1179C= MANE Select ENSP00000257863.3:p.Asp393=
ENST00000257863.8:c.1179C= ENSP00000257863.3:p.Asp393=
ENST00000379791.7:c.1140+244C= ENSP00000369117.3:n.1140+244C=
ENST00000550311.5:c.1179C= ENSP00000446661.1:p.Asp393=
ENST00000550839.1:c.270C= ENSP00000455338.1:p.Asp90=
ENST00000552233.5:n.767C=
NM_001164690.1:c.1179C= NP_001158162.1:p.Asp393=
NM_001164691.1:c.1140+244C= NP_001158163.1:n.1140+244C=
NM_020547.2:c.1179C= NP_065434.1:p.Asp393=
XM_011538173.1:c.1239C= XP_011536475.1:p.Asp413=
XM_011538174.1:c.1236C= XP_011536476.1:p.Asp412=
XM_011538175.1:c.1221C= XP_011536477.1:p.Asp407=
XM_011538176.1:c.1182C= XP_011536478.1:p.Asp394=
XM_011538177.1:c.1161C= XP_011536479.1:p.Asp387=
XM_011538178.1:c.1020C= XP_011536480.1:p.Asp340=
XM_011538179.1:c.1200+244C= XP_011536481.1:n.1200+244C=
XM_011538180.1:c.906C= XP_011536482.1:p.Asp302=
XM_011538181.1:c.903C= XP_011536483.1:p.Asp301=
XM_011538182.1:c.828C= XP_011536484.1:p.Asp276=
XM_011538183.1:c.1200+244C= XP_011536485.1:n.1200+244C=
XM_011538184.1:c.1220+224C= XP_011536486.1:n.1220+224C=
XM_011538185.1:c.856-1308C= XP_011536487.1:n.856-1308C=
XM_011538186.1:c.354C= XP_011536488.1:p.Asp118=
NM_001164690.2:c.1179C= NP_001158162.1:p.Asp393=
NM_001164691.2:c.1140+244C= NP_001158163.1:n.1140+244C=
NM_020547.3:c.1179C= MANE Select NP_065434.1:p.Asp393=
XM_011538183.2:c.1200+244C= XP_011536485.1:n.1200+244C=
XM_011538184.2:c.1220+224C= XP_011536486.1:n.1220+224C=
XM_011538186.3:c.354C= XP_011536488.1:p.Asp118=
XM_017019179.2:c.1239C= XP_016874668.1:p.Asp413=
XM_024448938.1:c.1143+244C= XP_024304706.1:n.1143+244C=
XR_002957309.1:n.1147C=
XR_002957310.1:n.1108+244C=
XR_002957311.1:n.1147C=
XR_002957312.1:n.1108+244C=