Canonical Allele Identifier: CA2631641536
Gene: PMM2 HGNC NCBI

Linked Data

gnomAD v4: 16-8797700-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797700A>T , CM000678.2:g.8797700A>T GRCh38
NC_000016.9:g.8891557A>T , CM000678.1:g.8891557A>T GRCh37
NC_000016.8:g.8799058A>T NCBI36
NG_009209.1:g.4888A>T
NG_033146.1:g.4949T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4099A>T ENSP00000457956.1:n.-15-4099A>T