Canonical Allele Identifier: CA2206128160
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797742T= , CM000678.2:g.8797742T= GRCh38
NC_000016.9:g.8891599T= , CM000678.1:g.8891599T= GRCh37
NC_000016.8:g.8799100T= NCBI36
NG_009209.1:g.4930T=
NG_033146.1:g.4907A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-141T= ENSP00000507849.1:n.-141T=
ENST00000566983.5:c.-15-4057T= ENSP00000457956.1:n.-15-4057T=