Canonical Allele Identifier: CA2700063940
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs2105672828
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219153C>T , CM000664.2:g.100219153C>T GRCh38
NC_000002.11:g.100835615C>T , CM000664.1:g.100835615C>T GRCh37
NC_000002.10:g.100202047C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10333C>T
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