Canonical Allele Identifier: CA445786876
Gene: PGAM5P1 HGNC NCBI
LINC01848 HGNC NCBI

Linked Data

gnomAD v4: 5-109885329-C-T
MyVariant Identifiers: chr5:g.109221030C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.109885329C>T , CM000667.2:g.109885329C>T GRCh38
NC_000005.9:g.109221030C>T , CM000667.1:g.109221030C>T GRCh37
NC_000005.8:g.109248929C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000518923.1:n.95G>A (PGAM5P1)
NR_033175.1:n.1096C>T (LINC01848)
Search 100 bp 5'
Search 100 bp 3'