Canonical Allele Identifier: CA2056319528
Gene: PGAM1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95565997T= , CM000674.2:g.95565997T= GRCh38
NC_000012.11:g.95959773T= , CM000674.1:g.95959773T= GRCh37
NC_000012.10:g.94483904T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000626376.2:n.219+14197T=