Canonical Allele Identifier: CA2036978811
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429907G= , CM000674.2:g.53429907G= GRCh38
NC_000012.11:g.53823691G= , CM000674.1:g.53823691G= GRCh37
NC_000012.10:g.52109958G= NCBI36
NG_015981.1:g.11053G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1217G= MANE Select ENSP00000257863.3:p.Arg406=
ENST00000257863.8:c.1217G= ENSP00000257863.3:p.Arg406=
ENST00000379791.7:c.1140+282G= ENSP00000369117.3:n.1140+282G=
ENST00000550311.5:c.1217G= ENSP00000446661.1:p.Arg406=
ENST00000550839.1:c.308G= ENSP00000455338.1:p.Arg103=
ENST00000552233.5:n.805G=
NM_001164690.1:c.1217G= NP_001158162.1:p.Arg406=
NM_001164691.1:c.1140+282G= NP_001158163.1:n.1140+282G=
NM_020547.2:c.1217G= NP_065434.1:p.Arg406=
XM_011538173.1:c.1277G= XP_011536475.1:p.Arg426=
XM_011538174.1:c.1274G= XP_011536476.1:p.Arg425=
XM_011538175.1:c.1259G= XP_011536477.1:p.Arg420=
XM_011538176.1:c.1220G= XP_011536478.1:p.Arg407=
XM_011538177.1:c.1199G= XP_011536479.1:p.Arg400=
XM_011538178.1:c.1058G= XP_011536480.1:p.Arg353=
XM_011538179.1:c.1200+282G= XP_011536481.1:n.1200+282G=
XM_011538180.1:c.944G= XP_011536482.1:p.Arg315=
XM_011538181.1:c.941G= XP_011536483.1:p.Arg314=
XM_011538182.1:c.866G= XP_011536484.1:p.Arg289=
XM_011538183.1:c.1201-239G= XP_011536485.1:n.1201-239G=
XM_011538184.1:c.1220+262G= XP_011536486.1:n.1220+262G=
XM_011538185.1:c.856-1270G= XP_011536487.1:n.856-1270G=
XM_011538186.1:c.392G= XP_011536488.1:p.Arg131=
NM_001164690.2:c.1217G= NP_001158162.1:p.Arg406=
NM_001164691.2:c.1140+282G= NP_001158163.1:n.1140+282G=
NM_020547.3:c.1217G= MANE Select NP_065434.1:p.Arg406=
XM_011538183.2:c.1201-239G= XP_011536485.1:n.1201-239G=
XM_011538184.2:c.1220+262G= XP_011536486.1:n.1220+262G=
XM_011538186.3:c.392G= XP_011536488.1:p.Arg131=
XM_017019179.2:c.1277G= XP_016874668.1:p.Arg426=
XM_024448938.1:c.1143+282G= XP_024304706.1:n.1143+282G=
XR_002957309.1:n.1185G=
XR_002957310.1:n.1109-239G=
XR_002957311.1:n.1185G=
XR_002957312.1:n.1108+282G=