Canonical Allele Identifier: CA1693197829
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1781823006
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845421G>A , CM000669.2:g.20845421G>A GRCh38
NC_000007.13:g.20885040G>A , CM000669.1:g.20885040G>A GRCh37
NC_000007.12:g.20851565G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9917G>A
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