Canonical Allele Identifier: CA2036978805
Gene: AMHR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53429903C= , CM000674.2:g.53429903C= GRCh38
NC_000012.11:g.53823687C= , CM000674.1:g.53823687C= GRCh37
NC_000012.10:g.52109954C= NCBI36
NG_015981.1:g.11049C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257863.9:c.1213C= MANE Select ENSP00000257863.3:p.Leu405=
ENST00000257863.8:c.1213C= ENSP00000257863.3:p.Leu405=
ENST00000379791.7:c.1140+278C= ENSP00000369117.3:n.1140+278C=
ENST00000550311.5:c.1213C= ENSP00000446661.1:p.Leu405=
ENST00000550839.1:c.304C= ENSP00000455338.1:p.Leu102=
ENST00000552233.5:n.801C=
NM_001164690.1:c.1213C= NP_001158162.1:p.Leu405=
NM_001164691.1:c.1140+278C= NP_001158163.1:n.1140+278C=
NM_020547.2:c.1213C= NP_065434.1:p.Leu405=
XM_011538173.1:c.1273C= XP_011536475.1:p.Leu425=
XM_011538174.1:c.1270C= XP_011536476.1:p.Leu424=
XM_011538175.1:c.1255C= XP_011536477.1:p.Leu419=
XM_011538176.1:c.1216C= XP_011536478.1:p.Leu406=
XM_011538177.1:c.1195C= XP_011536479.1:p.Leu399=
XM_011538178.1:c.1054C= XP_011536480.1:p.Leu352=
XM_011538179.1:c.1200+278C= XP_011536481.1:n.1200+278C=
XM_011538180.1:c.940C= XP_011536482.1:p.Leu314=
XM_011538181.1:c.937C= XP_011536483.1:p.Leu313=
XM_011538182.1:c.862C= XP_011536484.1:p.Leu288=
XM_011538183.1:c.1201-243C= XP_011536485.1:n.1201-243C=
XM_011538184.1:c.1220+258C= XP_011536486.1:n.1220+258C=
XM_011538185.1:c.856-1274C= XP_011536487.1:n.856-1274C=
XM_011538186.1:c.388C= XP_011536488.1:p.Leu130=
NM_001164690.2:c.1213C= NP_001158162.1:p.Leu405=
NM_001164691.2:c.1140+278C= NP_001158163.1:n.1140+278C=
NM_020547.3:c.1213C= MANE Select NP_065434.1:p.Leu405=
XM_011538183.2:c.1201-243C= XP_011536485.1:n.1201-243C=
XM_011538184.2:c.1220+258C= XP_011536486.1:n.1220+258C=
XM_011538186.3:c.388C= XP_011536488.1:p.Leu130=
XM_017019179.2:c.1273C= XP_016874668.1:p.Leu425=
XM_024448938.1:c.1143+278C= XP_024304706.1:n.1143+278C=
XR_002957309.1:n.1181C=
XR_002957310.1:n.1109-243C=
XR_002957311.1:n.1181C=
XR_002957312.1:n.1108+278C=