Canonical Allele Identifier: CA12335714
Gene: TARID HGNC NCBI
COSMIC:
COSN14876544 (not active)
MyVariant.info:
GRCh38 chr6:g.133546664G>A
GRCh37 chr6:g.133867802G>A
gnomAD v2:
6:133867802 G / A
gnomAD v3:
6:133546664 G / A
gnomAD v4:
chr6-133546664-G-A
Joint Max Group AF 0.30803383 (SAS)
Genomes Max Group AF 0.30803383 (SAS)
dbSNP:
9375969
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133546664G>A , CM000668.2:g.133546664G>A GRCh38
NC_000006.11:g.133867802G>A , CM000668.1:g.133867802G>A GRCh37
NC_000006.10:g.133909495G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.707-9306C>T
Search 100 bp 5'
Search 100 bp 3'