Canonical Allele Identifier: CA53081638
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs141251583

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219183A>C , CM000664.2:g.100219183A>C GRCh38
NC_000002.11:g.100835645A>C , CM000664.1:g.100835645A>C GRCh37
NC_000002.10:g.100202077A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10363A>C