Canonical Allele Identifier: CA535050372
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1210888793

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219234G>T , CM000664.2:g.100219234G>T GRCh38
NC_000002.11:g.100835696G>T , CM000664.1:g.100835696G>T GRCh37
NC_000002.10:g.100202128G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10414G>T