Canonical Allele Identifier: CA12740009
Gene: LINC00824 HGNC NCBI
COSMIC:
COSN17135820
COSN17139506
COSN17142464
COSN17146171
COSN17147065
COSN17147944
dbSNP:
10088218
gnomAD v2:
8:129543949 G / A
gnomAD v3:
8:128531703 G / A
gnomAD v4:
chr8-128531703-G-A
Joint Max Group AF 0.14760473 (MID)
Genomes Max Group AF 0.13916088 (AFR)
MyVariant.info:
GRCh38 chr8:g.128531703G>A
GRCh37 chr8:g.129543949G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531703G>A , CM000670.2:g.128531703G>A GRCh38
NC_000008.10:g.129543949G>A , CM000670.1:g.129543949G>A GRCh37
NC_000008.9:g.129613131G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+29367C>T
Search 100 bp 5'
Search 100 bp 3'