Canonical Allele Identifier: CA2206128111
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797662C= , CM000678.2:g.8797662C= GRCh38
NC_000016.9:g.8891519C= , CM000678.1:g.8891519C= GRCh37
NC_000016.8:g.8799020C= NCBI36
NG_009209.1:g.4850C=
NG_033146.1:g.4987G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4137C= ENSP00000457956.1:n.-15-4137C=