Canonical Allele Identifier: CA445786597
Gene: PGAM5P1 HGNC NCBI
LINC01848 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.109220932A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.109885231A>T , CM000667.2:g.109885231A>T GRCh38
NC_000005.9:g.109220932A>T , CM000667.1:g.109220932A>T GRCh37
NC_000005.8:g.109248831A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000518923.1:n.193T>A (PGAM5P1)
NR_033175.1:n.998A>T (LINC01848)