Canonical Allele Identifier: CA612948857
Gene: LINC00596 HGNC NCBI

Linked Data

dbSNP Id: rs1280688233
gnomAD v2: 14-24381527-C-T
gnomAD v3: 14-23912318-C-T
gnomAD v4: 14-23912318-C-T
MyVariant Identifiers: chr14:g.24381527C>T (hg19) chr14:g.23912318C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912318C>T , CM000676.2:g.23912318C>T GRCh38
NC_000014.8:g.24381527C>T , CM000676.1:g.24381527C>T GRCh37
NC_000014.7:g.23451367C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_429343.2:n.179-9606G>A
XR_001750659.1:n.196-9606G>A
XR_429343.3:n.196-9606G>A
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