Canonical Allele Identifier: CA693789297
Gene: PGAM1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1321836268
MyVariant Identifiers: chr12:g.95959707G>A (hg19) chr12:g.95565931G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.95565931G>A , CM000674.2:g.95565931G>A GRCh38
NC_000012.11:g.95959707G>A , CM000674.1:g.95959707G>A GRCh37
NC_000012.10:g.94483838G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000626376.2:n.219+14131G>A
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