Canonical Allele Identifier: CA185698770

Gene: PCAT2

Linked Data

• dbSNP Id: rs1042164673
• gnomAD v2: 8-128092088-T-G
• gnomAD v3: 8-127079843-T-G
• gnomAD v4: 8-127079843-T-G
• MyVariant Identifiers: chr8:g.128092088T>G (hg19) ; chr8:g.127079843T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127079843T>G , CM000670.2:g.127079843T>G	GRCh38
NC_000008.10:g.128092088T>G , CM000670.1:g.128092088T>G	GRCh37
NC_000008.9:g.128161270T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_119373.1:n.102-710A>C