Canonical Allele Identifier: CA754154386
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1414103941
MyVariant Identifiers: chr2:g.100835606T>G (hg19) chr2:g.100219144T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219144T>G , CM000664.2:g.100219144T>G GRCh38
NC_000002.11:g.100835606T>G , CM000664.1:g.100835606T>G GRCh37
NC_000002.10:g.100202038T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10324T>G
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