Canonical Allele Identifier: CA2123683157
Gene: LINC00596 HGNC NCBI

Linked Data

dbSNP Id: rs2031833871

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912295G>A , CM000676.2:g.23912295G>A GRCh38
NC_000014.8:g.24381504G>A , CM000676.1:g.24381504G>A GRCh37
NC_000014.7:g.23451344G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_429343.2:n.179-9583C>T
XR_001750659.1:n.196-9583C>T
XR_429343.3:n.196-9583C>T