Canonical Allele Identifier: CA385095009

Gene: AMHR2

Linked Data

• MyVariant Identifiers: chr12:g.53823624C>G (hg19) ; chr12:g.53429840C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53429840C>G , CM000674.2:g.53429840C>G	GRCh38
NC_000012.11:g.53823624C>G , CM000674.1:g.53823624C>G	GRCh37
NC_000012.10:g.52109891C>G	NCBI36
NG_015981.1:g.10986C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257863.9:c.1150C>G MANE Select	ENSP00000257863.3:p.Gln384Glu
ENST00000257863.8:c.1150C>G	ENSP00000257863.3:p.Gln384Glu
ENST00000379791.7:c.1140+215C>G	ENSP00000369117.3:n.1140+215C>G
ENST00000550311.5:c.1150C>G	ENSP00000446661.1:p.Gln384Glu
ENST00000550839.1:c.241C>G	ENSP00000455338.1:p.Gln81Glu
ENST00000552233.5:n.738C>G
NM_001164690.1:c.1150C>G	NP_001158162.1:p.Gln384Glu
NM_001164691.1:c.1140+215C>G	NP_001158163.1:n.1140+215C>G
NM_020547.2:c.1150C>G	NP_065434.1:p.Gln384Glu
XM_011538173.1:c.1210C>G	XP_011536475.1:p.Gln404Glu
XM_011538174.1:c.1207C>G	XP_011536476.1:p.Gln403Glu
XM_011538175.1:c.1192C>G	XP_011536477.1:p.Gln398Glu
XM_011538176.1:c.1153C>G	XP_011536478.1:p.Gln385Glu
XM_011538177.1:c.1132C>G	XP_011536479.1:p.Gln378Glu
XM_011538178.1:c.991C>G	XP_011536480.1:p.Gln331Glu
XM_011538179.1:c.1200+215C>G	XP_011536481.1:n.1200+215C>G
XM_011538180.1:c.877C>G	XP_011536482.1:p.Gln293Glu
XM_011538181.1:c.874C>G	XP_011536483.1:p.Gln292Glu
XM_011538182.1:c.799C>G	XP_011536484.1:p.Gln267Glu
XM_011538183.1:c.1200+215C>G	XP_011536485.1:n.1200+215C>G
XM_011538184.1:c.1220+195C>G	XP_011536486.1:n.1220+195C>G
XM_011538185.1:c.856-1337C>G	XP_011536487.1:n.856-1337C>G
XM_011538186.1:c.325C>G	XP_011536488.1:p.Gln109Glu
NM_001164690.2:c.1150C>G	NP_001158162.1:p.Gln384Glu
NM_001164691.2:c.1140+215C>G	NP_001158163.1:n.1140+215C>G
NM_020547.3:c.1150C>G MANE Select	NP_065434.1:p.Gln384Glu
XM_011538183.2:c.1200+215C>G	XP_011536485.1:n.1200+215C>G
XM_011538184.2:c.1220+195C>G	XP_011536486.1:n.1220+195C>G
XM_011538186.3:c.325C>G	XP_011536488.1:p.Gln109Glu
XM_017019179.2:c.1210C>G	XP_016874668.1:p.Gln404Glu
XM_024448938.1:c.1143+215C>G	XP_024304706.1:n.1143+215C>G
XR_002957309.1:n.1118C>G
XR_002957310.1:n.1108+215C>G
XR_002957311.1:n.1118C>G
XR_002957312.1:n.1108+215C>G