Canonical Allele Identifier: CA2056319590
Gene: PGAM1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95566073T= , CM000674.2:g.95566073T= GRCh38
NC_000012.11:g.95959849T= , CM000674.1:g.95959849T= GRCh37
NC_000012.10:g.94483980T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000626376.2:n.219+14273T=