Canonical Allele Identifier: CA2056319325
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs2077781880

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95565830C>T , CM000674.2:g.95565830C>T GRCh38
NC_000012.11:g.95959606C>T , CM000674.1:g.95959606C>T GRCh37
NC_000012.10:g.94483737C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000626376.2:n.219+14030C>T