Canonical Allele Identifier: CA2206128198
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797795C= , CM000678.2:g.8797795C= GRCh38
NC_000016.9:g.8891652C= , CM000678.1:g.8891652C= GRCh37
NC_000016.8:g.8799153C= NCBI36
NG_009209.1:g.4983C=
NG_033146.1:g.4854G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-88C= ENSP00000507849.1:n.-88C=
ENST00000566983.5:c.-15-4004C= ENSP00000457956.1:n.-15-4004C=