Canonical Allele Identifier: CA1693234770
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1783253427
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954818G>C , CM000669.2:g.20954818G>C GRCh38
NC_000007.13:g.20994437G>C , CM000669.1:g.20994437G>C GRCh37
NC_000007.12:g.20960962G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66050G>C
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