Canonical Allele Identifier: CA403243223
Gene: AMH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251754T>A , CM000681.2:g.2251754T>A GRCh38
NC_000019.9:g.2251753T>A , CM000681.1:g.2251753T>A GRCh37
NC_000019.8:g.2202753T>A NCBI36
NG_012190.1:g.7641T>A
NG_032853.1:g.9670A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1480T>A MANE Select ENSP00000221496.2:p.Trp494Arg
ENST00000221496.4:c.1480T>A ENSP00000221496.2:p.Trp494Arg
NM_000479.3:c.1480T>A NP_000470.2:p.Trp494Arg
NM_000479.4:c.1480T>A NP_000470.2:p.Trp494Arg
NM_000479.5:c.1480T>A MANE Select NP_000470.3:p.Trp494Arg