Canonical Allele Identifier: CA185698771

Gene: PCAT2

Linked Data

• dbSNP Id: rs573392900
• gnomAD v3: 8-127079846-G-A
• gnomAD v4: 8-127079846-G-A
• MyVariant Identifiers: chr8:g.128092091G>A (hg19) ; chr8:g.127079846G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127079846G>A , CM000670.2:g.127079846G>A	GRCh38
NC_000008.10:g.128092091G>A , CM000670.1:g.128092091G>A	GRCh37
NC_000008.9:g.128161273G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_119373.1:n.102-713C>T