Canonical Allele Identifier: CA385095227

Gene: AMHR2

Linked Data

• dbSNP Id: rs1939961213
• MyVariant Identifiers: chr12:g.53823670A>G (hg19) ; chr12:g.53429886A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429886A>G , CM000674.2:g.53429886A>G	GRCh38
NC_000012.11:g.53823670A>G , CM000674.1:g.53823670A>G	GRCh37
NC_000012.10:g.52109937A>G	NCBI36
NG_015981.1:g.11032A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1196A>G MANE Select	ENSP00000257863.3:p.Gln399Arg
ENST00000257863.8:c.1196A>G	ENSP00000257863.3:p.Gln399Arg
ENST00000379791.7:c.1140+261A>G	ENSP00000369117.3:n.1140+261A>G
ENST00000550311.5:c.1196A>G	ENSP00000446661.1:p.Gln399Arg
ENST00000550839.1:c.287A>G	ENSP00000455338.1:p.Gln96Arg
ENST00000552233.5:n.784A>G
NM_001164690.1:c.1196A>G	NP_001158162.1:p.Gln399Arg
NM_001164691.1:c.1140+261A>G	NP_001158163.1:n.1140+261A>G
NM_020547.2:c.1196A>G	NP_065434.1:p.Gln399Arg
XM_011538173.1:c.1256A>G	XP_011536475.1:p.Gln419Arg
XM_011538174.1:c.1253A>G	XP_011536476.1:p.Gln418Arg
XM_011538175.1:c.1238A>G	XP_011536477.1:p.Gln413Arg
XM_011538176.1:c.1199A>G	XP_011536478.1:p.Gln400Arg
XM_011538177.1:c.1178A>G	XP_011536479.1:p.Gln393Arg
XM_011538178.1:c.1037A>G	XP_011536480.1:p.Gln346Arg
XM_011538179.1:c.1200+261A>G	XP_011536481.1:n.1200+261A>G
XM_011538180.1:c.923A>G	XP_011536482.1:p.Gln308Arg
XM_011538181.1:c.920A>G	XP_011536483.1:p.Gln307Arg
XM_011538182.1:c.845A>G	XP_011536484.1:p.Gln282Arg
XM_011538183.1:c.1201-260A>G	XP_011536485.1:n.1201-260A>G
XM_011538184.1:c.1220+241A>G	XP_011536486.1:n.1220+241A>G
XM_011538185.1:c.856-1291A>G	XP_011536487.1:n.856-1291A>G
XM_011538186.1:c.371A>G	XP_011536488.1:p.Gln124Arg
NM_001164690.2:c.1196A>G	NP_001158162.1:p.Gln399Arg
NM_001164691.2:c.1140+261A>G	NP_001158163.1:n.1140+261A>G
NM_020547.3:c.1196A>G MANE Select	NP_065434.1:p.Gln399Arg
XM_011538183.2:c.1201-260A>G	XP_011536485.1:n.1201-260A>G
XM_011538184.2:c.1220+241A>G	XP_011536486.1:n.1220+241A>G
XM_011538186.3:c.371A>G	XP_011536488.1:p.Gln124Arg
XM_017019179.2:c.1256A>G	XP_016874668.1:p.Gln419Arg
XM_024448938.1:c.1143+261A>G	XP_024304706.1:n.1143+261A>G
XR_002957309.1:n.1164A>G
XR_002957310.1:n.1109-260A>G
XR_002957311.1:n.1164A>G
XR_002957312.1:n.1108+261A>G