Canonical Allele Identifier: CA1274240143
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694222354

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219276A>G , CM000664.2:g.100219276A>G GRCh38
NC_000002.11:g.100835738A>G , CM000664.1:g.100835738A>G GRCh37
NC_000002.10:g.100202170A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+10456A>G