Canonical Allele Identifier: CA2206128167
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797749A= , CM000678.2:g.8797749A= GRCh38
NC_000016.9:g.8891606A= , CM000678.1:g.8891606A= GRCh37
NC_000016.8:g.8799107A= NCBI36
NG_009209.1:g.4937A=
NG_033146.1:g.4900T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682008.1:c.-134A= ENSP00000507849.1:n.-134A=
ENST00000566983.5:c.-15-4050A= ENSP00000457956.1:n.-15-4050A=