Canonical Allele Identifier: CA612948858
Gene: LINC00596 HGNC NCBI

Linked Data

dbSNP Id: rs1312741154
gnomAD v2: 14-24381547-G-A
gnomAD v3: 14-23912338-G-A
gnomAD v4: 14-23912338-G-A
MyVariant Identifiers: chr14:g.24381547G>A (hg19) chr14:g.23912338G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912338G>A , CM000676.2:g.23912338G>A GRCh38
NC_000014.8:g.24381547G>A , CM000676.1:g.24381547G>A GRCh37
NC_000014.7:g.23451387G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_429343.2:n.179-9626C>T
XR_001750659.1:n.196-9626C>T
XR_429343.3:n.196-9626C>T
Search 100 bp 5'
Search 100 bp 3'