Canonical Allele Identifier: CA11157426
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs10198446

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219150T>C , CM000664.2:g.100219150T>C GRCh38
NC_000002.11:g.100835612T>C , CM000664.1:g.100835612T>C GRCh37
NC_000002.10:g.100202044T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+10330T>C