Canonical Allele Identifier: CA13974588
Gene: LINC00596 HGNC NCBI

Linked Data

dbSNP Id: rs12436436

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912306T>C , CM000676.2:g.23912306T>C GRCh38
NC_000014.8:g.24381515T>C , CM000676.1:g.24381515T>C GRCh37
NC_000014.7:g.23451355T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_429343.2:n.179-9594A>G
XR_001750659.1:n.196-9594A>G
XR_429343.3:n.196-9594A>G