Canonical Allele Identifier: CA2206128176
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797765G= , CM000678.2:g.8797765G= GRCh38
NC_000016.9:g.8891622G= , CM000678.1:g.8891622G= GRCh37
NC_000016.8:g.8799123G= NCBI36
NG_009209.1:g.4953G=
NG_033146.1:g.4884C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-118G= ENSP00000507849.1:n.-118G=
ENST00000566983.5:c.-15-4034G= ENSP00000457956.1:n.-15-4034G=