Canonical Allele Identifier: CA445786587
Gene: PGAM5P1 HGNC NCBI
LINC01848 HGNC NCBI

Linked Data

gnomAD v4: 5-109885228-T-C
MyVariant Identifiers: chr5:g.109220929T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.109885228T>C , CM000667.2:g.109885228T>C GRCh38
NC_000005.9:g.109220929T>C , CM000667.1:g.109220929T>C GRCh37
NC_000005.8:g.109248828T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000518923.1:n.196A>G (PGAM5P1)
NR_033175.1:n.995T>C (LINC01848)
Search 100 bp 5'
Search 100 bp 3'