Canonical Allele Identifier: CA155638043
Gene: LINC01162 HGNC NCBI

Linked Data

dbSNP Id: rs987916704
gnomAD v2: 7-20884982-T-C
gnomAD v3: 7-20845363-T-C
gnomAD v4: 7-20845363-T-C
MyVariant Identifiers: chr7:g.20884982T>C (hg19) chr7:g.20845363T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.20845363T>C , CM000669.2:g.20845363T>C GRCh38
NC_000007.13:g.20884982T>C , CM000669.1:g.20884982T>C GRCh37
NC_000007.12:g.20851507T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126381.1:n.74+9859T>C
Search 100 bp 5'
Search 100 bp 3'