Canonical Allele Identifier: CA2318204420
Gene: AMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251577C= , CM000681.2:g.2251577C= GRCh38
NC_000019.9:g.2251576C= , CM000681.1:g.2251576C= GRCh37
NC_000019.8:g.2202576C= NCBI36
NG_012190.1:g.7464C=
NG_032853.1:g.9847G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1303C= MANE Select ENSP00000221496.2:p.Arg435=
ENST00000221496.4:c.1303C= ENSP00000221496.2:p.Arg435=
ENST00000589313.2:n.1656C=
NM_000479.3:c.1303C= NP_000470.2:p.Arg435=
NM_000479.4:c.1303C= NP_000470.2:p.Arg435=
NM_000479.5:c.1303C= MANE Select NP_000470.3:p.Arg435=