Canonical Allele Identifier: CA445786606
Gene: PGAM5P1 HGNC NCBI
LINC01848 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.109220935T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.109885234T>G , CM000667.2:g.109885234T>G GRCh38
NC_000005.9:g.109220935T>G , CM000667.1:g.109220935T>G GRCh37
NC_000005.8:g.109248834T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000518923.1:n.190A>C (PGAM5P1)
NR_033175.1:n.1001T>G (LINC01848)