Canonical Allele Identifier: CA385094979

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823615G>T (hg19) ; chr12:g.53429831G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429831G>T , CM000674.2:g.53429831G>T	GRCh38
NC_000012.11:g.53823615G>T , CM000674.1:g.53823615G>T	GRCh37
NC_000012.10:g.52109882G>T	NCBI36
NG_015981.1:g.10977G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1141G>T MANE Select	ENSP00000257863.3:p.Ala381Ser
ENST00000257863.8:c.1141G>T	ENSP00000257863.3:p.Ala381Ser
ENST00000379791.7:c.1140+206G>T	ENSP00000369117.3:n.1140+206G>T
ENST00000550311.5:c.1141G>T	ENSP00000446661.1:p.Ala381Ser
ENST00000550839.1:c.232G>T	ENSP00000455338.1:p.Ala78Ser
ENST00000552233.5:n.729G>T
NM_001164690.1:c.1141G>T	NP_001158162.1:p.Ala381Ser
NM_001164691.1:c.1140+206G>T	NP_001158163.1:n.1140+206G>T
NM_020547.2:c.1141G>T	NP_065434.1:p.Ala381Ser
XM_011538173.1:c.1201G>T	XP_011536475.1:p.Ala401Ser
XM_011538174.1:c.1198G>T	XP_011536476.1:p.Ala400Ser
XM_011538175.1:c.1183G>T	XP_011536477.1:p.Ala395Ser
XM_011538176.1:c.1144G>T	XP_011536478.1:p.Ala382Ser
XM_011538177.1:c.1123G>T	XP_011536479.1:p.Ala375Ser
XM_011538178.1:c.982G>T	XP_011536480.1:p.Ala328Ser
XM_011538179.1:c.1200+206G>T	XP_011536481.1:n.1200+206G>T
XM_011538180.1:c.868G>T	XP_011536482.1:p.Ala290Ser
XM_011538181.1:c.865G>T	XP_011536483.1:p.Ala289Ser
XM_011538182.1:c.790G>T	XP_011536484.1:p.Ala264Ser
XM_011538183.1:c.1200+206G>T	XP_011536485.1:n.1200+206G>T
XM_011538184.1:c.1220+186G>T	XP_011536486.1:n.1220+186G>T
XM_011538185.1:c.856-1346G>T	XP_011536487.1:n.856-1346G>T
XM_011538186.1:c.316G>T	XP_011536488.1:p.Ala106Ser
NM_001164690.2:c.1141G>T	NP_001158162.1:p.Ala381Ser
NM_001164691.2:c.1140+206G>T	NP_001158163.1:n.1140+206G>T
NM_020547.3:c.1141G>T MANE Select	NP_065434.1:p.Ala381Ser
XM_011538183.2:c.1200+206G>T	XP_011536485.1:n.1200+206G>T
XM_011538184.2:c.1220+186G>T	XP_011536486.1:n.1220+186G>T
XM_011538186.3:c.316G>T	XP_011536488.1:p.Ala106Ser
XM_017019179.2:c.1201G>T	XP_016874668.1:p.Ala401Ser
XM_024448938.1:c.1143+206G>T	XP_024304706.1:n.1143+206G>T
XR_002957309.1:n.1109G>T
XR_002957310.1:n.1108+206G>T
XR_002957311.1:n.1109G>T
XR_002957312.1:n.1108+206G>T