Canonical Allele Identifier: CA385095147

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823652A>G (hg19) ; chr12:g.53429868A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429868A>G , CM000674.2:g.53429868A>G	GRCh38
NC_000012.11:g.53823652A>G , CM000674.1:g.53823652A>G	GRCh37
NC_000012.10:g.52109919A>G	NCBI36
NG_015981.1:g.11014A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1178A>G MANE Select	ENSP00000257863.3:p.Asp393Gly
ENST00000257863.8:c.1178A>G	ENSP00000257863.3:p.Asp393Gly
ENST00000379791.7:c.1140+243A>G	ENSP00000369117.3:n.1140+243A>G
ENST00000550311.5:c.1178A>G	ENSP00000446661.1:p.Asp393Gly
ENST00000550839.1:c.269A>G	ENSP00000455338.1:p.Asp90Gly
ENST00000552233.5:n.766A>G
NM_001164690.1:c.1178A>G	NP_001158162.1:p.Asp393Gly
NM_001164691.1:c.1140+243A>G	NP_001158163.1:n.1140+243A>G
NM_020547.2:c.1178A>G	NP_065434.1:p.Asp393Gly
XM_011538173.1:c.1238A>G	XP_011536475.1:p.Asp413Gly
XM_011538174.1:c.1235A>G	XP_011536476.1:p.Asp412Gly
XM_011538175.1:c.1220A>G	XP_011536477.1:p.Asp407Gly
XM_011538176.1:c.1181A>G	XP_011536478.1:p.Asp394Gly
XM_011538177.1:c.1160A>G	XP_011536479.1:p.Asp387Gly
XM_011538178.1:c.1019A>G	XP_011536480.1:p.Asp340Gly
XM_011538179.1:c.1200+243A>G	XP_011536481.1:n.1200+243A>G
XM_011538180.1:c.905A>G	XP_011536482.1:p.Asp302Gly
XM_011538181.1:c.902A>G	XP_011536483.1:p.Asp301Gly
XM_011538182.1:c.827A>G	XP_011536484.1:p.Asp276Gly
XM_011538183.1:c.1200+243A>G	XP_011536485.1:n.1200+243A>G
XM_011538184.1:c.1220+223A>G	XP_011536486.1:n.1220+223A>G
XM_011538185.1:c.856-1309A>G	XP_011536487.1:n.856-1309A>G
XM_011538186.1:c.353A>G	XP_011536488.1:p.Asp118Gly
NM_001164690.2:c.1178A>G	NP_001158162.1:p.Asp393Gly
NM_001164691.2:c.1140+243A>G	NP_001158163.1:n.1140+243A>G
NM_020547.3:c.1178A>G MANE Select	NP_065434.1:p.Asp393Gly
XM_011538183.2:c.1200+243A>G	XP_011536485.1:n.1200+243A>G
XM_011538184.2:c.1220+223A>G	XP_011536486.1:n.1220+223A>G
XM_011538186.3:c.353A>G	XP_011536488.1:p.Asp118Gly
XM_017019179.2:c.1238A>G	XP_016874668.1:p.Asp413Gly
XM_024448938.1:c.1143+243A>G	XP_024304706.1:n.1143+243A>G
XR_002957309.1:n.1146A>G
XR_002957310.1:n.1108+243A>G
XR_002957311.1:n.1146A>G
XR_002957312.1:n.1108+243A>G