Canonical Allele Identifier: CA403242150
Gene: AMH HGNC NCBI

Linked Data

gnomAD v4: 19-2251392-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251392C>A , CM000681.2:g.2251392C>A GRCh38
NC_000019.9:g.2251391C>A , CM000681.1:g.2251391C>A GRCh37
NC_000019.8:g.2202391C>A NCBI36
NG_012190.1:g.7279C>A
NG_032853.1:g.10032G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1118C>A MANE Select ENSP00000221496.2:p.Thr373Lys
ENST00000221496.4:c.1118C>A ENSP00000221496.2:p.Thr373Lys
ENST00000589313.2:n.1471C>A
NM_000479.3:c.1118C>A NP_000470.2:p.Thr373Lys
NM_000479.4:c.1118C>A NP_000470.2:p.Thr373Lys
NM_000479.5:c.1118C>A MANE Select NP_000470.3:p.Thr373Lys