Canonical Allele Identifier: CA2036978809
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429906C= , CM000674.2:g.53429906C= GRCh38
NC_000012.11:g.53823690C= , CM000674.1:g.53823690C= GRCh37
NC_000012.10:g.52109957C= NCBI36
NG_015981.1:g.11052C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1216C= MANE Select ENSP00000257863.3:p.Arg406=
ENST00000257863.8:c.1216C= ENSP00000257863.3:p.Arg406=
ENST00000379791.7:c.1140+281C= ENSP00000369117.3:n.1140+281C=
ENST00000550311.5:c.1216C= ENSP00000446661.1:p.Arg406=
ENST00000550839.1:c.307C= ENSP00000455338.1:p.Arg103=
ENST00000552233.5:n.804C=
NM_001164690.1:c.1216C= NP_001158162.1:p.Arg406=
NM_001164691.1:c.1140+281C= NP_001158163.1:n.1140+281C=
NM_020547.2:c.1216C= NP_065434.1:p.Arg406=
XM_011538173.1:c.1276C= XP_011536475.1:p.Arg426=
XM_011538174.1:c.1273C= XP_011536476.1:p.Arg425=
XM_011538175.1:c.1258C= XP_011536477.1:p.Arg420=
XM_011538176.1:c.1219C= XP_011536478.1:p.Arg407=
XM_011538177.1:c.1198C= XP_011536479.1:p.Arg400=
XM_011538178.1:c.1057C= XP_011536480.1:p.Arg353=
XM_011538179.1:c.1200+281C= XP_011536481.1:n.1200+281C=
XM_011538180.1:c.943C= XP_011536482.1:p.Arg315=
XM_011538181.1:c.940C= XP_011536483.1:p.Arg314=
XM_011538182.1:c.865C= XP_011536484.1:p.Arg289=
XM_011538183.1:c.1201-240C= XP_011536485.1:n.1201-240C=
XM_011538184.1:c.1220+261C= XP_011536486.1:n.1220+261C=
XM_011538185.1:c.856-1271C= XP_011536487.1:n.856-1271C=
XM_011538186.1:c.391C= XP_011536488.1:p.Arg131=
NM_001164690.2:c.1216C= NP_001158162.1:p.Arg406=
NM_001164691.2:c.1140+281C= NP_001158163.1:n.1140+281C=
NM_020547.3:c.1216C= MANE Select NP_065434.1:p.Arg406=
XM_011538183.2:c.1201-240C= XP_011536485.1:n.1201-240C=
XM_011538184.2:c.1220+261C= XP_011536486.1:n.1220+261C=
XM_011538186.3:c.391C= XP_011536488.1:p.Arg131=
XM_017019179.2:c.1276C= XP_016874668.1:p.Arg426=
XM_024448938.1:c.1143+281C= XP_024304706.1:n.1143+281C=
XR_002957309.1:n.1184C=
XR_002957310.1:n.1109-240C=
XR_002957311.1:n.1184C=
XR_002957312.1:n.1108+281C=