Canonical Allele Identifier: CA961103953
Gene: LINC00596 HGNC NCBI

Linked Data

dbSNP Id: rs2031834422
gnomAD v3: 14-23912312-T-A
gnomAD v4: 14-23912312-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912312T>A , CM000676.2:g.23912312T>A GRCh38
NC_000014.8:g.24381521T>A , CM000676.1:g.24381521T>A GRCh37
NC_000014.7:g.23451361T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_429343.2:n.179-9600A>T
XR_001750659.1:n.196-9600A>T
XR_429343.3:n.196-9600A>T
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