Canonical Allele Identifier: CA2036978758
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429840C= , CM000674.2:g.53429840C= GRCh38
NC_000012.11:g.53823624C= , CM000674.1:g.53823624C= GRCh37
NC_000012.10:g.52109891C= NCBI36
NG_015981.1:g.10986C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1150C= MANE Select ENSP00000257863.3:p.Gln384=
ENST00000257863.8:c.1150C= ENSP00000257863.3:p.Gln384=
ENST00000379791.7:c.1140+215C= ENSP00000369117.3:n.1140+215C=
ENST00000550311.5:c.1150C= ENSP00000446661.1:p.Gln384=
ENST00000550839.1:c.241C= ENSP00000455338.1:p.Gln81=
ENST00000552233.5:n.738C=
NM_001164690.1:c.1150C= NP_001158162.1:p.Gln384=
NM_001164691.1:c.1140+215C= NP_001158163.1:n.1140+215C=
NM_020547.2:c.1150C= NP_065434.1:p.Gln384=
XM_011538173.1:c.1210C= XP_011536475.1:p.Gln404=
XM_011538174.1:c.1207C= XP_011536476.1:p.Gln403=
XM_011538175.1:c.1192C= XP_011536477.1:p.Gln398=
XM_011538176.1:c.1153C= XP_011536478.1:p.Gln385=
XM_011538177.1:c.1132C= XP_011536479.1:p.Gln378=
XM_011538178.1:c.991C= XP_011536480.1:p.Gln331=
XM_011538179.1:c.1200+215C= XP_011536481.1:n.1200+215C=
XM_011538180.1:c.877C= XP_011536482.1:p.Gln293=
XM_011538181.1:c.874C= XP_011536483.1:p.Gln292=
XM_011538182.1:c.799C= XP_011536484.1:p.Gln267=
XM_011538183.1:c.1200+215C= XP_011536485.1:n.1200+215C=
XM_011538184.1:c.1220+195C= XP_011536486.1:n.1220+195C=
XM_011538185.1:c.856-1337C= XP_011536487.1:n.856-1337C=
XM_011538186.1:c.325C= XP_011536488.1:p.Gln109=
NM_001164690.2:c.1150C= NP_001158162.1:p.Gln384=
NM_001164691.2:c.1140+215C= NP_001158163.1:n.1140+215C=
NM_020547.3:c.1150C= MANE Select NP_065434.1:p.Gln384=
XM_011538183.2:c.1200+215C= XP_011536485.1:n.1200+215C=
XM_011538184.2:c.1220+195C= XP_011536486.1:n.1220+195C=
XM_011538186.3:c.325C= XP_011536488.1:p.Gln109=
XM_017019179.2:c.1210C= XP_016874668.1:p.Gln404=
XM_024448938.1:c.1143+215C= XP_024304706.1:n.1143+215C=
XR_002957309.1:n.1118C=
XR_002957310.1:n.1108+215C=
XR_002957311.1:n.1118C=
XR_002957312.1:n.1108+215C=