Canonical Allele Identifier: CA385095599

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823760C>A (hg19) ; chr12:g.53429976C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429976C>A , CM000674.2:g.53429976C>A	GRCh38
NC_000012.11:g.53823760C>A , CM000674.1:g.53823760C>A	GRCh37
NC_000012.10:g.52110027C>A	NCBI36
NG_015981.1:g.11122C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1286C>A MANE Select	ENSP00000257863.3:p.Pro429His
ENST00000257863.8:c.1286C>A	ENSP00000257863.3:p.Pro429His
ENST00000379791.7:c.1140+351C>A	ENSP00000369117.3:n.1140+351C>A
ENST00000550311.5:c.1286C>A	ENSP00000446661.1:p.Pro429His
ENST00000550839.1:c.377C>A	ENSP00000455338.1:p.Pro126His
ENST00000552233.5:n.874C>A
NM_001164690.1:c.1286C>A	NP_001158162.1:p.Pro429His
NM_001164691.1:c.1140+351C>A	NP_001158163.1:n.1140+351C>A
NM_020547.2:c.1286C>A	NP_065434.1:p.Pro429His
XM_011538173.1:c.1346C>A	XP_011536475.1:p.Pro449His
XM_011538174.1:c.1343C>A	XP_011536476.1:p.Pro448His
XM_011538175.1:c.1328C>A	XP_011536477.1:p.Pro443His
XM_011538176.1:c.1289C>A	XP_011536478.1:p.Pro430His
XM_011538177.1:c.1268C>A	XP_011536479.1:p.Pro423His
XM_011538178.1:c.1127C>A	XP_011536480.1:p.Pro376His
XM_011538179.1:c.1200+351C>A	XP_011536481.1:n.1200+351C>A
XM_011538180.1:c.1013C>A	XP_011536482.1:p.Pro338His
XM_011538181.1:c.1010C>A	XP_011536483.1:p.Pro337His
XM_011538182.1:c.935C>A	XP_011536484.1:p.Pro312His
XM_011538183.1:c.1201-170C>A	XP_011536485.1:n.1201-170C>A
XM_011538184.1:c.1220+331C>A	XP_011536486.1:n.1220+331C>A
XM_011538185.1:c.856-1201C>A	XP_011536487.1:n.856-1201C>A
XM_011538186.1:c.461C>A	XP_011536488.1:p.Pro154His
NM_001164690.2:c.1286C>A	NP_001158162.1:p.Pro429His
NM_001164691.2:c.1140+351C>A	NP_001158163.1:n.1140+351C>A
NM_020547.3:c.1286C>A MANE Select	NP_065434.1:p.Pro429His
XM_011538183.2:c.1201-170C>A	XP_011536485.1:n.1201-170C>A
XM_011538184.2:c.1220+331C>A	XP_011536486.1:n.1220+331C>A
XM_011538186.3:c.461C>A	XP_011536488.1:p.Pro154His
XM_017019179.2:c.1346C>A	XP_016874668.1:p.Pro449His
XM_024448938.1:c.1143+351C>A	XP_024304706.1:n.1143+351C>A
XR_002957309.1:n.1254C>A
XR_002957310.1:n.1109-170C>A
XR_002957311.1:n.1254C>A
XR_002957312.1:n.1108+351C>A