Canonical Allele Identifier: CA2206128139
Gene: PMM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.8797704G= , CM000678.2:g.8797704G= GRCh38
NC_000016.9:g.8891561G= , CM000678.1:g.8891561G= GRCh37
NC_000016.8:g.8799062G= NCBI36
NG_009209.1:g.4892G=
NG_033146.1:g.4945C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000566983.5:c.-15-4095G= ENSP00000457956.1:n.-15-4095G=