Canonical Allele Identifier: CA385095377

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823711T>G (hg19) ; chr12:g.53429927T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429927T>G , CM000674.2:g.53429927T>G	GRCh38
NC_000012.11:g.53823711T>G , CM000674.1:g.53823711T>G	GRCh37
NC_000012.10:g.52109978T>G	NCBI36
NG_015981.1:g.11073T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1237T>G MANE Select	ENSP00000257863.3:p.Leu413Val
ENST00000257863.8:c.1237T>G	ENSP00000257863.3:p.Leu413Val
ENST00000379791.7:c.1140+302T>G	ENSP00000369117.3:n.1140+302T>G
ENST00000550311.5:c.1237T>G	ENSP00000446661.1:p.Leu413Val
ENST00000550839.1:c.328T>G	ENSP00000455338.1:p.Leu110Val
ENST00000552233.5:n.825T>G
NM_001164690.1:c.1237T>G	NP_001158162.1:p.Leu413Val
NM_001164691.1:c.1140+302T>G	NP_001158163.1:n.1140+302T>G
NM_020547.2:c.1237T>G	NP_065434.1:p.Leu413Val
XM_011538173.1:c.1297T>G	XP_011536475.1:p.Leu433Val
XM_011538174.1:c.1294T>G	XP_011536476.1:p.Leu432Val
XM_011538175.1:c.1279T>G	XP_011536477.1:p.Leu427Val
XM_011538176.1:c.1240T>G	XP_011536478.1:p.Leu414Val
XM_011538177.1:c.1219T>G	XP_011536479.1:p.Leu407Val
XM_011538178.1:c.1078T>G	XP_011536480.1:p.Leu360Val
XM_011538179.1:c.1200+302T>G	XP_011536481.1:n.1200+302T>G
XM_011538180.1:c.964T>G	XP_011536482.1:p.Leu322Val
XM_011538181.1:c.961T>G	XP_011536483.1:p.Leu321Val
XM_011538182.1:c.886T>G	XP_011536484.1:p.Leu296Val
XM_011538183.1:c.1201-219T>G	XP_011536485.1:n.1201-219T>G
XM_011538184.1:c.1220+282T>G	XP_011536486.1:n.1220+282T>G
XM_011538185.1:c.856-1250T>G	XP_011536487.1:n.856-1250T>G
XM_011538186.1:c.412T>G	XP_011536488.1:p.Leu138Val
NM_001164690.2:c.1237T>G	NP_001158162.1:p.Leu413Val
NM_001164691.2:c.1140+302T>G	NP_001158163.1:n.1140+302T>G
NM_020547.3:c.1237T>G MANE Select	NP_065434.1:p.Leu413Val
XM_011538183.2:c.1201-219T>G	XP_011536485.1:n.1201-219T>G
XM_011538184.2:c.1220+282T>G	XP_011536486.1:n.1220+282T>G
XM_011538186.3:c.412T>G	XP_011536488.1:p.Leu138Val
XM_017019179.2:c.1297T>G	XP_016874668.1:p.Leu433Val
XM_024448938.1:c.1143+302T>G	XP_024304706.1:n.1143+302T>G
XR_002957309.1:n.1205T>G
XR_002957310.1:n.1109-219T>G
XR_002957311.1:n.1205T>G
XR_002957312.1:n.1108+302T>G