Canonical Allele Identifier: CA2206128109
Gene: PMM2 HGNC NCBI

Linked Data

dbSNP Id: rs2060585852
gnomAD v4: 16-8797657-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797657G>A , CM000678.2:g.8797657G>A GRCh38
NC_000016.9:g.8891514G>A , CM000678.1:g.8891514G>A GRCh37
NC_000016.8:g.8799015G>A NCBI36
NG_009209.1:g.4845G>A
NG_033146.1:g.4992C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4142G>A ENSP00000457956.1:n.-15-4142G>A