Canonical Allele Identifier: CA847138762
Gene: PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1372467696
MyVariant Identifiers: chr8:g.128092101A>C (hg19) chr8:g.127079856A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079856A>C , CM000670.2:g.127079856A>C GRCh38
NC_000008.10:g.128092101A>C , CM000670.1:g.128092101A>C GRCh37
NC_000008.9:g.128161283A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-723T>G
Search 100 bp 5'
Search 100 bp 3'