Canonical Allele Identifier: CA836611535
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs1481788590
gnomAD v3: 7-20954862-C-T
gnomAD v4: 7-20954862-C-T
MyVariant Identifiers: chr7:g.20994481C>T (hg19) chr7:g.20954862C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20954862C>T , CM000669.2:g.20954862C>T GRCh38
NC_000007.13:g.20994481C>T , CM000669.1:g.20994481C>T GRCh37
NC_000007.12:g.20961006C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.152-66006C>T
Search 100 bp 5'
Search 100 bp 3'