Canonical Allele Identifier: CA2036978816
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429910G= , CM000674.2:g.53429910G= GRCh38
NC_000012.11:g.53823694G= , CM000674.1:g.53823694G= GRCh37
NC_000012.10:g.52109961G= NCBI36
NG_015981.1:g.11056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1220G= MANE Select ENSP00000257863.3:p.Arg407=
ENST00000257863.8:c.1220G= ENSP00000257863.3:p.Arg407=
ENST00000379791.7:c.1140+285G= ENSP00000369117.3:n.1140+285G=
ENST00000550311.5:c.1220G= ENSP00000446661.1:p.Arg407=
ENST00000550839.1:c.311G= ENSP00000455338.1:p.Arg104=
ENST00000552233.5:n.808G=
NM_001164690.1:c.1220G= NP_001158162.1:p.Arg407=
NM_001164691.1:c.1140+285G= NP_001158163.1:n.1140+285G=
NM_020547.2:c.1220G= NP_065434.1:p.Arg407=
XM_011538173.1:c.1280G= XP_011536475.1:p.Arg427=
XM_011538174.1:c.1277G= XP_011536476.1:p.Arg426=
XM_011538175.1:c.1262G= XP_011536477.1:p.Arg421=
XM_011538176.1:c.1223G= XP_011536478.1:p.Arg408=
XM_011538177.1:c.1202G= XP_011536479.1:p.Arg401=
XM_011538178.1:c.1061G= XP_011536480.1:p.Arg354=
XM_011538179.1:c.1200+285G= XP_011536481.1:n.1200+285G=
XM_011538180.1:c.947G= XP_011536482.1:p.Arg316=
XM_011538181.1:c.944G= XP_011536483.1:p.Arg315=
XM_011538182.1:c.869G= XP_011536484.1:p.Arg290=
XM_011538183.1:c.1201-236G= XP_011536485.1:n.1201-236G=
XM_011538184.1:c.1220+265G= XP_011536486.1:n.1220+265G=
XM_011538185.1:c.856-1267G= XP_011536487.1:n.856-1267G=
XM_011538186.1:c.395G= XP_011536488.1:p.Arg132=
NM_001164690.2:c.1220G= NP_001158162.1:p.Arg407=
NM_001164691.2:c.1140+285G= NP_001158163.1:n.1140+285G=
NM_020547.3:c.1220G= MANE Select NP_065434.1:p.Arg407=
XM_011538183.2:c.1201-236G= XP_011536485.1:n.1201-236G=
XM_011538184.2:c.1220+265G= XP_011536486.1:n.1220+265G=
XM_011538186.3:c.395G= XP_011536488.1:p.Arg132=
XM_017019179.2:c.1280G= XP_016874668.1:p.Arg427=
XM_024448938.1:c.1143+285G= XP_024304706.1:n.1143+285G=
XR_002957309.1:n.1188G=
XR_002957310.1:n.1109-236G=
XR_002957311.1:n.1188G=
XR_002957312.1:n.1108+285G=