Canonical Allele Identifier: CA2631641523
Gene: PMM2 HGNC NCBI

Linked Data

gnomAD v4: 16-8797696-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797696C>A , CM000678.2:g.8797696C>A GRCh38
NC_000016.9:g.8891553C>A , CM000678.1:g.8891553C>A GRCh37
NC_000016.8:g.8799054C>A NCBI36
NG_009209.1:g.4884C>A
NG_033146.1:g.4953G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4103C>A ENSP00000457956.1:n.-15-4103C>A