Canonical Allele Identifier: CA2318204568

Gene: AMH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251819C= , CM000681.2:g.2251819C=	GRCh38
NC_000019.9:g.2251818C= , CM000681.1:g.2251818C=	GRCh37
NC_000019.8:g.2202818C=	NCBI36
NG_012190.1:g.7706C=
NG_032853.1:g.9605G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000221496.5:c.1545C= MANE Select	ENSP00000221496.2:p.Val515=
ENST00000221496.4:c.1545C=	ENSP00000221496.2:p.Val515=
NM_000479.3:c.1545C=	NP_000470.2:p.Ala515=
NM_000479.4:c.1545C=	NP_000470.2:p.Ala515=
NM_000479.5:c.1545C= MANE Select	NP_000470.3:p.Val515=