Canonical Allele Identifier: CA2631641487
Gene: PMM2 HGNC NCBI

Linked Data

gnomAD v4: 16-8797680-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797680G>T , CM000678.2:g.8797680G>T GRCh38
NC_000016.9:g.8891537G>T , CM000678.1:g.8891537G>T GRCh37
NC_000016.8:g.8799038G>T NCBI36
NG_009209.1:g.4868G>T
NG_033146.1:g.4969C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4119G>T ENSP00000457956.1:n.-15-4119G>T