Canonical Allele Identifier: CA2631641449
Gene: PMM2 HGNC NCBI

Linked Data

gnomAD v4: 16-8797663-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797663C>A , CM000678.2:g.8797663C>A GRCh38
NC_000016.9:g.8891520C>A , CM000678.1:g.8891520C>A GRCh37
NC_000016.8:g.8799021C>A NCBI36
NG_009209.1:g.4851C>A
NG_033146.1:g.4986G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4136C>A ENSP00000457956.1:n.-15-4136C>A
Search 100 bp 5'
Search 100 bp 3'