Canonical Allele Identifier: CA445786886
Gene: PGAM5P1 HGNC NCBI
LINC01848 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.109221034G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.109885333G>A , CM000667.2:g.109885333G>A GRCh38
NC_000005.9:g.109221034G>A , CM000667.1:g.109221034G>A GRCh37
NC_000005.8:g.109248933G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000518923.1:n.91C>T (PGAM5P1)
NR_033175.1:n.1100G>A (LINC01848)
Search 100 bp 5'
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