Canonical Allele Identifier: CA12249917
Gene: LINC01312 HGNC NCBI
TARID HGNC NCBI
COSMIC:
COSN15632920 (not active)
COSN16063146 (not active)
MyVariant.info:
GRCh38 chr6:g.133837662T>C
GRCh37 chr6:g.134158800T>C
gnomAD v2:
6:134158800 T / C
gnomAD v3:
6:133837662 T / C
gnomAD v4:
chr6-133837662-T-C
Joint Max Group AF 0.44841262 (EAS)
Genomes Max Group AF 0.44841262 (EAS)
dbSNP:
1208285
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133837662T>C , CM000668.2:g.133837662T>C GRCh38
NC_000006.11:g.134158800T>C , CM000668.1:g.134158800T>C GRCh37
NC_000006.10:g.134200493T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_027030.1:n.659T>C (LINC01312)
NR_109982.1:n.478+8215A>G (TARID)
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