Canonical Allele Identifier: CA185698769
Gene: PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs71520630
gnomAD v2: 8-128092084-A-G
gnomAD v3: 8-127079839-A-G
gnomAD v4: 8-127079839-A-G
MyVariant Identifiers: chr8:g.128092084A>G (hg19) chr8:g.127079839A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079839A>G , CM000670.2:g.127079839A>G GRCh38
NC_000008.10:g.128092084A>G , CM000670.1:g.128092084A>G GRCh37
NC_000008.9:g.128161266A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-706T>C
Search 100 bp 5'
Search 100 bp 3'