Canonical Allele Identifier: CA385095606

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823762G>C (hg19) ; chr12:g.53429978G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429978G>C , CM000674.2:g.53429978G>C	GRCh38
NC_000012.11:g.53823762G>C , CM000674.1:g.53823762G>C	GRCh37
NC_000012.10:g.52110029G>C	NCBI36
NG_015981.1:g.11124G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1288G>C MANE Select	ENSP00000257863.3:p.Asp430His
ENST00000257863.8:c.1288G>C	ENSP00000257863.3:p.Asp430His
ENST00000379791.7:c.1140+353G>C	ENSP00000369117.3:n.1140+353G>C
ENST00000550311.5:c.1288G>C	ENSP00000446661.1:p.Ala430Pro
ENST00000550839.1:c.379G>C	ENSP00000455338.1:p.Asp127His
ENST00000552233.5:n.876G>C
NM_001164690.1:c.1288G>C	NP_001158162.1:p.Ala430Pro
NM_001164691.1:c.1140+353G>C	NP_001158163.1:n.1140+353G>C
NM_020547.2:c.1288G>C	NP_065434.1:p.Asp430His
XM_011538173.1:c.1348G>C	XP_011536475.1:p.Asp450His
XM_011538174.1:c.1345G>C	XP_011536476.1:p.Asp449His
XM_011538175.1:c.1330G>C	XP_011536477.1:p.Asp444His
XM_011538176.1:c.1291G>C	XP_011536478.1:p.Asp431His
XM_011538177.1:c.1270G>C	XP_011536479.1:p.Asp424His
XM_011538178.1:c.1129G>C	XP_011536480.1:p.Asp377His
XM_011538179.1:c.1200+353G>C	XP_011536481.1:n.1200+353G>C
XM_011538180.1:c.1015G>C	XP_011536482.1:p.Asp339His
XM_011538181.1:c.1012G>C	XP_011536483.1:p.Asp338His
XM_011538182.1:c.937G>C	XP_011536484.1:p.Asp313His
XM_011538183.1:c.1201-168G>C	XP_011536485.1:n.1201-168G>C
XM_011538184.1:c.1220+333G>C	XP_011536486.1:n.1220+333G>C
XM_011538185.1:c.856-1199G>C	XP_011536487.1:n.856-1199G>C
XM_011538186.1:c.463G>C	XP_011536488.1:p.Asp155His
NM_001164690.2:c.1288G>C	NP_001158162.1:p.Ala430Pro
NM_001164691.2:c.1140+353G>C	NP_001158163.1:n.1140+353G>C
NM_020547.3:c.1288G>C MANE Select	NP_065434.1:p.Asp430His
XM_011538183.2:c.1201-168G>C	XP_011536485.1:n.1201-168G>C
XM_011538184.2:c.1220+333G>C	XP_011536486.1:n.1220+333G>C
XM_011538186.3:c.463G>C	XP_011536488.1:p.Asp155His
XM_017019179.2:c.1348G>C	XP_016874668.1:p.Gly450Arg
XM_024448938.1:c.1143+353G>C	XP_024304706.1:n.1143+353G>C
XR_002957309.1:n.1256G>C
XR_002957310.1:n.1109-168G>C
XR_002957311.1:n.1256G>C
XR_002957312.1:n.1108+353G>C