Canonical Allele Identifier: CA48805975
Gene: LINC01122 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_033873.1:n.248-40649A>C
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