Canonical Allele Identifier: CA12059942

Gene: PGAM5P1 LINC01848

Linked Data

• dbSNP Id: rs112724034
• gnomAD v2: 5-109221026-C-T
• gnomAD v3: 5-109885325-C-T
• gnomAD v4: 5-109885325-C-T
• MyVariant Identifiers: chr5:g.109221026C>T (hg19) ; chr5:g.109885325C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.109885325C>T , CM000667.2:g.109885325C>T	GRCh38
NC_000005.9:g.109221026C>T , CM000667.1:g.109221026C>T	GRCh37
NC_000005.8:g.109248925C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518923.1:n.99G>A (PGAM5P1)
NR_033175.1:n.1092C>T (LINC01848)