Canonical Allele Identifier: CA385095025

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823627A>T (hg19) ; chr12:g.53429843A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429843A>T , CM000674.2:g.53429843A>T	GRCh38
NC_000012.11:g.53823627A>T , CM000674.1:g.53823627A>T	GRCh37
NC_000012.10:g.52109894A>T	NCBI36
NG_015981.1:g.10989A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1153A>T MANE Select	ENSP00000257863.3:p.Arg385Trp
ENST00000257863.8:c.1153A>T	ENSP00000257863.3:p.Arg385Trp
ENST00000379791.7:c.1140+218A>T	ENSP00000369117.3:n.1140+218A>T
ENST00000550311.5:c.1153A>T	ENSP00000446661.1:p.Arg385Trp
ENST00000550839.1:c.244A>T	ENSP00000455338.1:p.Arg82Trp
ENST00000552233.5:n.741A>T
NM_001164690.1:c.1153A>T	NP_001158162.1:p.Arg385Trp
NM_001164691.1:c.1140+218A>T	NP_001158163.1:n.1140+218A>T
NM_020547.2:c.1153A>T	NP_065434.1:p.Arg385Trp
XM_011538173.1:c.1213A>T	XP_011536475.1:p.Arg405Trp
XM_011538174.1:c.1210A>T	XP_011536476.1:p.Arg404Trp
XM_011538175.1:c.1195A>T	XP_011536477.1:p.Arg399Trp
XM_011538176.1:c.1156A>T	XP_011536478.1:p.Arg386Trp
XM_011538177.1:c.1135A>T	XP_011536479.1:p.Arg379Trp
XM_011538178.1:c.994A>T	XP_011536480.1:p.Arg332Trp
XM_011538179.1:c.1200+218A>T	XP_011536481.1:n.1200+218A>T
XM_011538180.1:c.880A>T	XP_011536482.1:p.Arg294Trp
XM_011538181.1:c.877A>T	XP_011536483.1:p.Arg293Trp
XM_011538182.1:c.802A>T	XP_011536484.1:p.Arg268Trp
XM_011538183.1:c.1200+218A>T	XP_011536485.1:n.1200+218A>T
XM_011538184.1:c.1220+198A>T	XP_011536486.1:n.1220+198A>T
XM_011538185.1:c.856-1334A>T	XP_011536487.1:n.856-1334A>T
XM_011538186.1:c.328A>T	XP_011536488.1:p.Arg110Trp
NM_001164690.2:c.1153A>T	NP_001158162.1:p.Arg385Trp
NM_001164691.2:c.1140+218A>T	NP_001158163.1:n.1140+218A>T
NM_020547.3:c.1153A>T MANE Select	NP_065434.1:p.Arg385Trp
XM_011538183.2:c.1200+218A>T	XP_011536485.1:n.1200+218A>T
XM_011538184.2:c.1220+198A>T	XP_011536486.1:n.1220+198A>T
XM_011538186.3:c.328A>T	XP_011536488.1:p.Arg110Trp
XM_017019179.2:c.1213A>T	XP_016874668.1:p.Arg405Trp
XM_024448938.1:c.1143+218A>T	XP_024304706.1:n.1143+218A>T
XR_002957309.1:n.1121A>T
XR_002957310.1:n.1108+218A>T
XR_002957311.1:n.1121A>T
XR_002957312.1:n.1108+218A>T