ClinGen Allele Registry
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Canonical Allele Identifier:
CA1099137354
Gene: LINC01162
HGNC
NCBI
Linked Data
dbSNP Id:
rs1781822720
gnomAD v3:
7-20845389-T-G
gnomAD v4:
7-20845389-T-G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.20845389T>G , CM000669.2:g.20845389T>G
GRCh38
NC_000007.13:g.20885008T>G , CM000669.1:g.20885008T>G
GRCh37
NC_000007.12:g.20851533T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_126381.1:n.74+9885T>G
Search 100 bp 5'
Search 100 bp 3'