Canonical Allele Identifier: CA2318204675

Gene: AMH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251968G= , CM000681.2:g.2251968G=	GRCh38
NC_000019.9:g.2251967G= , CM000681.1:g.2251967G=	GRCh37
NC_000019.8:g.2202967G=	NCBI36
NG_012190.1:g.7855G=
NG_032853.1:g.9456C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.*11G= MANE Select	ENSP00000221496.2:n.*11G=
ENST00000221496.4:c.*11G=	ENSP00000221496.2:n.*11G=
NM_000479.3:c.*11G=	NP_000470.2:n.*11G=
NM_000479.4:c.*11G=	NP_000470.2:n.*11G=
NM_000479.5:c.*11G= MANE Select	NP_000470.3:n.*11G=