Canonical Allele Identifier: CA2318204508

Gene: AMH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251718A= , CM000681.2:g.2251718A=	GRCh38
NC_000019.9:g.2251717A= , CM000681.1:g.2251717A=	GRCh37
NC_000019.8:g.2202717A=	NCBI36
NG_012190.1:g.7605A=
NG_032853.1:g.9706T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.1444A= MANE Select	ENSP00000221496.2:p.Thr482=
ENST00000221496.4:c.1444A=	ENSP00000221496.2:p.Thr482=
NM_000479.3:c.1444A=	NP_000470.2:p.Thr482=
NM_000479.4:c.1444A=	NP_000470.2:p.Thr482=
NM_000479.5:c.1444A= MANE Select	NP_000470.3:p.Thr482=