Canonical Allele Identifier: CA445786590
Gene: PGAM5P1 HGNC NCBI
LINC01848 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.109220930C>A (hg19)

Genomic Alleles

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

Transcript Alleles

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