Canonical Allele Identifier: CA1034234464
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694220121

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219126A>C , CM000664.2:g.100219126A>C GRCh38
NC_000002.11:g.100835588A>C , CM000664.1:g.100835588A>C GRCh37
NC_000002.10:g.100202020A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10306A>C