Canonical Allele Identifier: CA385094993

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823619G>C (hg19) ; chr12:g.53429835G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429835G>C , CM000674.2:g.53429835G>C	GRCh38
NC_000012.11:g.53823619G>C , CM000674.1:g.53823619G>C	GRCh37
NC_000012.10:g.52109886G>C	NCBI36
NG_015981.1:g.10981G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257863.9:c.1145G>C MANE Select	ENSP00000257863.3:p.Gly382Ala
ENST00000257863.8:c.1145G>C	ENSP00000257863.3:p.Gly382Ala
ENST00000379791.7:c.1140+210G>C	ENSP00000369117.3:n.1140+210G>C
ENST00000550311.5:c.1145G>C	ENSP00000446661.1:p.Gly382Ala
ENST00000550839.1:c.236G>C	ENSP00000455338.1:p.Gly79Ala
ENST00000552233.5:n.733G>C
NM_001164690.1:c.1145G>C	NP_001158162.1:p.Gly382Ala
NM_001164691.1:c.1140+210G>C	NP_001158163.1:n.1140+210G>C
NM_020547.2:c.1145G>C	NP_065434.1:p.Gly382Ala
XM_011538173.1:c.1205G>C	XP_011536475.1:p.Gly402Ala
XM_011538174.1:c.1202G>C	XP_011536476.1:p.Gly401Ala
XM_011538175.1:c.1187G>C	XP_011536477.1:p.Gly396Ala
XM_011538176.1:c.1148G>C	XP_011536478.1:p.Gly383Ala
XM_011538177.1:c.1127G>C	XP_011536479.1:p.Gly376Ala
XM_011538178.1:c.986G>C	XP_011536480.1:p.Gly329Ala
XM_011538179.1:c.1200+210G>C	XP_011536481.1:n.1200+210G>C
XM_011538180.1:c.872G>C	XP_011536482.1:p.Gly291Ala
XM_011538181.1:c.869G>C	XP_011536483.1:p.Gly290Ala
XM_011538182.1:c.794G>C	XP_011536484.1:p.Gly265Ala
XM_011538183.1:c.1200+210G>C	XP_011536485.1:n.1200+210G>C
XM_011538184.1:c.1220+190G>C	XP_011536486.1:n.1220+190G>C
XM_011538185.1:c.856-1342G>C	XP_011536487.1:n.856-1342G>C
XM_011538186.1:c.320G>C	XP_011536488.1:p.Gly107Ala
NM_001164690.2:c.1145G>C	NP_001158162.1:p.Gly382Ala
NM_001164691.2:c.1140+210G>C	NP_001158163.1:n.1140+210G>C
NM_020547.3:c.1145G>C MANE Select	NP_065434.1:p.Gly382Ala
XM_011538183.2:c.1200+210G>C	XP_011536485.1:n.1200+210G>C
XM_011538184.2:c.1220+190G>C	XP_011536486.1:n.1220+190G>C
XM_011538186.3:c.320G>C	XP_011536488.1:p.Gly107Ala
XM_017019179.2:c.1205G>C	XP_016874668.1:p.Gly402Ala
XM_024448938.1:c.1143+210G>C	XP_024304706.1:n.1143+210G>C
XR_002957309.1:n.1113G>C
XR_002957310.1:n.1108+210G>C
XR_002957311.1:n.1113G>C
XR_002957312.1:n.1108+210G>C