Canonical Allele Identifier: CA385095100

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823642G>C (hg19) ; chr12:g.53429858G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429858G>C , CM000674.2:g.53429858G>C	GRCh38
NC_000012.11:g.53823642G>C , CM000674.1:g.53823642G>C	GRCh37
NC_000012.10:g.52109909G>C	NCBI36
NG_015981.1:g.11004G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1168G>C MANE Select	ENSP00000257863.3:p.Glu390Gln
ENST00000257863.8:c.1168G>C	ENSP00000257863.3:p.Glu390Gln
ENST00000379791.7:c.1140+233G>C	ENSP00000369117.3:n.1140+233G>C
ENST00000550311.5:c.1168G>C	ENSP00000446661.1:p.Glu390Gln
ENST00000550839.1:c.259G>C	ENSP00000455338.1:p.Glu87Gln
ENST00000552233.5:n.756G>C
NM_001164690.1:c.1168G>C	NP_001158162.1:p.Glu390Gln
NM_001164691.1:c.1140+233G>C	NP_001158163.1:n.1140+233G>C
NM_020547.2:c.1168G>C	NP_065434.1:p.Glu390Gln
XM_011538173.1:c.1228G>C	XP_011536475.1:p.Glu410Gln
XM_011538174.1:c.1225G>C	XP_011536476.1:p.Glu409Gln
XM_011538175.1:c.1210G>C	XP_011536477.1:p.Glu404Gln
XM_011538176.1:c.1171G>C	XP_011536478.1:p.Glu391Gln
XM_011538177.1:c.1150G>C	XP_011536479.1:p.Glu384Gln
XM_011538178.1:c.1009G>C	XP_011536480.1:p.Glu337Gln
XM_011538179.1:c.1200+233G>C	XP_011536481.1:n.1200+233G>C
XM_011538180.1:c.895G>C	XP_011536482.1:p.Glu299Gln
XM_011538181.1:c.892G>C	XP_011536483.1:p.Glu298Gln
XM_011538182.1:c.817G>C	XP_011536484.1:p.Glu273Gln
XM_011538183.1:c.1200+233G>C	XP_011536485.1:n.1200+233G>C
XM_011538184.1:c.1220+213G>C	XP_011536486.1:n.1220+213G>C
XM_011538185.1:c.856-1319G>C	XP_011536487.1:n.856-1319G>C
XM_011538186.1:c.343G>C	XP_011536488.1:p.Glu115Gln
NM_001164690.2:c.1168G>C	NP_001158162.1:p.Glu390Gln
NM_001164691.2:c.1140+233G>C	NP_001158163.1:n.1140+233G>C
NM_020547.3:c.1168G>C MANE Select	NP_065434.1:p.Glu390Gln
XM_011538183.2:c.1200+233G>C	XP_011536485.1:n.1200+233G>C
XM_011538184.2:c.1220+213G>C	XP_011536486.1:n.1220+213G>C
XM_011538186.3:c.343G>C	XP_011536488.1:p.Glu115Gln
XM_017019179.2:c.1228G>C	XP_016874668.1:p.Glu410Gln
XM_024448938.1:c.1143+233G>C	XP_024304706.1:n.1143+233G>C
XR_002957309.1:n.1136G>C
XR_002957310.1:n.1108+233G>C
XR_002957311.1:n.1136G>C
XR_002957312.1:n.1108+233G>C