Canonical Allele Identifier: CA2576558521

Gene: AMH

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251982C>G , CM000681.2:g.2251982C>G	GRCh38
NC_000019.9:g.2251981C>G , CM000681.1:g.2251981C>G	GRCh37
NC_000019.8:g.2202981C>G	NCBI36
NG_012190.1:g.7869C>G
NG_032853.1:g.9442G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.*25C>G MANE Select	ENSP00000221496.2:n.*25C>G
ENST00000221496.4:c.*25C>G	ENSP00000221496.2:n.*25C>G
NM_000479.3:c.*25C>G	NP_000470.2:n.*25C>G
NM_000479.4:c.*25C>G	NP_000470.2:n.*25C>G
NM_000479.5:c.*25C>G MANE Select	NP_000470.3:n.*25C>G