Canonical Allele Identifier: CA2206128168
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797753C= , CM000678.2:g.8797753C= GRCh38
NC_000016.9:g.8891610C= , CM000678.1:g.8891610C= GRCh37
NC_000016.8:g.8799111C= NCBI36
NG_009209.1:g.4941C=
NG_033146.1:g.4896G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-130C= ENSP00000507849.1:n.-130C=
ENST00000566983.5:c.-15-4046C= ENSP00000457956.1:n.-15-4046C=