Canonical Allele Identifier: CA1254043240
Gene: LINC01122 HGNC NCBI

Linked Data

dbSNP Id: rs6719884

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.58809781A>G , CM000664.2:g.58809781A>G GRCh38
NC_000002.11:g.59036916A>G , CM000664.1:g.59036916A>G GRCh37
NC_000002.10:g.58890420A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033873.1:n.248-40649A>G