Canonical Allele Identifier: CA836611533
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1471386053
gnomAD v3: 7-20954856-G-C
gnomAD v4: 7-20954856-G-C
MyVariant Identifiers: chr7:g.20994475G>C (hg19) chr7:g.20954856G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954856G>C , CM000669.2:g.20954856G>C GRCh38
NC_000007.13:g.20994475G>C , CM000669.1:g.20994475G>C GRCh37
NC_000007.12:g.20961000G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66012G>C
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