Canonical Allele Identifier: CA2502219170
Gene: LINC01122 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58809764G>T , CM000664.2:g.58809764G>T GRCh38
NC_000002.11:g.59036899G>T , CM000664.1:g.59036899G>T GRCh37
NC_000002.10:g.58890403G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.248-40666G>T
Search 100 bp 5'
Search 100 bp 3'