Canonical Allele Identifier: CA2036978795
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429892G= , CM000674.2:g.53429892G= GRCh38
NC_000012.11:g.53823676G= , CM000674.1:g.53823676G= GRCh37
NC_000012.10:g.52109943G= NCBI36
NG_015981.1:g.11038G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1202G= MANE Select ENSP00000257863.3:p.Trp401=
ENST00000257863.8:c.1202G= ENSP00000257863.3:p.Trp401=
ENST00000379791.7:c.1140+267G= ENSP00000369117.3:n.1140+267G=
ENST00000550311.5:c.1202G= ENSP00000446661.1:p.Trp401=
ENST00000550839.1:c.293G= ENSP00000455338.1:p.Trp98=
ENST00000552233.5:n.790G=
NM_001164690.1:c.1202G= NP_001158162.1:p.Trp401=
NM_001164691.1:c.1140+267G= NP_001158163.1:n.1140+267G=
NM_020547.2:c.1202G= NP_065434.1:p.Trp401=
XM_011538173.1:c.1262G= XP_011536475.1:p.Trp421=
XM_011538174.1:c.1259G= XP_011536476.1:p.Trp420=
XM_011538175.1:c.1244G= XP_011536477.1:p.Trp415=
XM_011538176.1:c.1205G= XP_011536478.1:p.Trp402=
XM_011538177.1:c.1184G= XP_011536479.1:p.Trp395=
XM_011538178.1:c.1043G= XP_011536480.1:p.Trp348=
XM_011538179.1:c.1200+267G= XP_011536481.1:n.1200+267G=
XM_011538180.1:c.929G= XP_011536482.1:p.Trp310=
XM_011538181.1:c.926G= XP_011536483.1:p.Trp309=
XM_011538182.1:c.851G= XP_011536484.1:p.Trp284=
XM_011538183.1:c.1201-254G= XP_011536485.1:n.1201-254G=
XM_011538184.1:c.1220+247G= XP_011536486.1:n.1220+247G=
XM_011538185.1:c.856-1285G= XP_011536487.1:n.856-1285G=
XM_011538186.1:c.377G= XP_011536488.1:p.Trp126=
NM_001164690.2:c.1202G= NP_001158162.1:p.Trp401=
NM_001164691.2:c.1140+267G= NP_001158163.1:n.1140+267G=
NM_020547.3:c.1202G= MANE Select NP_065434.1:p.Trp401=
XM_011538183.2:c.1201-254G= XP_011536485.1:n.1201-254G=
XM_011538184.2:c.1220+247G= XP_011536486.1:n.1220+247G=
XM_011538186.3:c.377G= XP_011536488.1:p.Trp126=
XM_017019179.2:c.1262G= XP_016874668.1:p.Trp421=
XM_024448938.1:c.1143+267G= XP_024304706.1:n.1143+267G=
XR_002957309.1:n.1170G=
XR_002957310.1:n.1109-254G=
XR_002957311.1:n.1170G=
XR_002957312.1:n.1108+267G=