Canonical Allele Identifier: CA2036978752
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429838C= , CM000674.2:g.53429838C= GRCh38
NC_000012.11:g.53823622C= , CM000674.1:g.53823622C= GRCh37
NC_000012.10:g.52109889C= NCBI36
NG_015981.1:g.10984C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1148C= MANE Select ENSP00000257863.3:p.Thr383=
ENST00000257863.8:c.1148C= ENSP00000257863.3:p.Thr383=
ENST00000379791.7:c.1140+213C= ENSP00000369117.3:n.1140+213C=
ENST00000550311.5:c.1148C= ENSP00000446661.1:p.Thr383=
ENST00000550839.1:c.239C= ENSP00000455338.1:p.Thr80=
ENST00000552233.5:n.736C=
NM_001164690.1:c.1148C= NP_001158162.1:p.Thr383=
NM_001164691.1:c.1140+213C= NP_001158163.1:n.1140+213C=
NM_020547.2:c.1148C= NP_065434.1:p.Thr383=
XM_011538173.1:c.1208C= XP_011536475.1:p.Thr403=
XM_011538174.1:c.1205C= XP_011536476.1:p.Thr402=
XM_011538175.1:c.1190C= XP_011536477.1:p.Thr397=
XM_011538176.1:c.1151C= XP_011536478.1:p.Thr384=
XM_011538177.1:c.1130C= XP_011536479.1:p.Thr377=
XM_011538178.1:c.989C= XP_011536480.1:p.Thr330=
XM_011538179.1:c.1200+213C= XP_011536481.1:n.1200+213C=
XM_011538180.1:c.875C= XP_011536482.1:p.Thr292=
XM_011538181.1:c.872C= XP_011536483.1:p.Thr291=
XM_011538182.1:c.797C= XP_011536484.1:p.Thr266=
XM_011538183.1:c.1200+213C= XP_011536485.1:n.1200+213C=
XM_011538184.1:c.1220+193C= XP_011536486.1:n.1220+193C=
XM_011538185.1:c.856-1339C= XP_011536487.1:n.856-1339C=
XM_011538186.1:c.323C= XP_011536488.1:p.Thr108=
NM_001164690.2:c.1148C= NP_001158162.1:p.Thr383=
NM_001164691.2:c.1140+213C= NP_001158163.1:n.1140+213C=
NM_020547.3:c.1148C= MANE Select NP_065434.1:p.Thr383=
XM_011538183.2:c.1200+213C= XP_011536485.1:n.1200+213C=
XM_011538184.2:c.1220+193C= XP_011536486.1:n.1220+193C=
XM_011538186.3:c.323C= XP_011536488.1:p.Thr108=
XM_017019179.2:c.1208C= XP_016874668.1:p.Thr403=
XM_024448938.1:c.1143+213C= XP_024304706.1:n.1143+213C=
XR_002957309.1:n.1116C=
XR_002957310.1:n.1108+213C=
XR_002957311.1:n.1116C=
XR_002957312.1:n.1108+213C=