Canonical Allele Identifier: CA403242733
Gene: AMH HGNC NCBI

Linked Data

gnomAD v4: 19-2251584-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251584A>T , CM000681.2:g.2251584A>T GRCh38
NC_000019.9:g.2251583A>T , CM000681.1:g.2251583A>T GRCh37
NC_000019.8:g.2202583A>T NCBI36
NG_012190.1:g.7471A>T
NG_032853.1:g.9840T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1310A>T MANE Select ENSP00000221496.2:p.Glu437Val
ENST00000221496.4:c.1310A>T ENSP00000221496.2:p.Glu437Val
ENST00000589313.2:n.1663A>T
NM_000479.3:c.1310A>T NP_000470.2:p.Glu437Val
NM_000479.4:c.1310A>T NP_000470.2:p.Glu437Val
NM_000479.5:c.1310A>T MANE Select NP_000470.3:p.Glu437Val