Canonical Allele Identifier: CA2583853212

Gene: AMH

Linked Data

• gnomAD v4: 19-2251966-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.2251966C>T , CM000681.2:g.2251966C>T	GRCh38
NC_000019.9:g.2251965C>T , CM000681.1:g.2251965C>T	GRCh37
NC_000019.8:g.2202965C>T	NCBI36
NG_012190.1:g.7853C>T
NG_032853.1:g.9458G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221496.5:c.*9C>T MANE Select	ENSP00000221496.2:n.*9C>T
ENST00000221496.4:c.*9C>T	ENSP00000221496.2:n.*9C>T
NM_000479.3:c.*9C>T	NP_000470.2:n.*9C>T
NM_000479.4:c.*9C>T	NP_000470.2:n.*9C>T
NM_000479.5:c.*9C>T MANE Select	NP_000470.3:n.*9C>T