Canonical Allele Identifier: CA2318204252

Gene: AMH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251330C= , CM000681.2:g.2251330C=	GRCh38
NC_000019.9:g.2251329C= , CM000681.1:g.2251329C=	GRCh37
NC_000019.8:g.2202329C=	NCBI36
NG_012190.1:g.7217C=
NG_032853.1:g.10094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.1056C= MANE Select	ENSP00000221496.2:p.Pro352=
ENST00000221496.4:c.1056C=	ENSP00000221496.2:p.Pro352=
ENST00000589313.2:n.1409C=
NM_000479.3:c.1056C=	NP_000470.2:p.Pro352=
NM_000479.4:c.1056C=	NP_000470.2:p.Pro352=
NM_000479.5:c.1056C= MANE Select	NP_000470.3:p.Pro352=