Canonical Allele Identifier: CA2318204567
Gene: AMH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2251818T= , CM000681.2:g.2251818T= GRCh38
NC_000019.9:g.2251817T= , CM000681.1:g.2251817T= GRCh37
NC_000019.8:g.2202817T= NCBI36
NG_032853.1:g.9606A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221496.5:c.1544T= MANE Select ENSP00000221496.2:p.Val515=
ENST00000221496.4:c.1544T= ENSP00000221496.2:p.Val515=
NM_000479.5:c.1544T= MANE Select NP_000470.3:p.Val515=