Canonical Allele Identifier: CA1571973221
Gene: PGAM5P1 HGNC NCBI
LINC01848 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.109885229C= , CM000667.2:g.109885229C= GRCh38
NC_000005.9:g.109220930C= , CM000667.1:g.109220930C= GRCh37
NC_000005.8:g.109248829C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000518923.1:n.195G= (PGAM5P1)
NR_033175.1:n.996C= (LINC01848)