Canonical Allele Identifier: CA12335714

Gene: TARID

Linked Data

• dbSNP Id: rs9375969
• gnomAD v2: 6-133867802-G-A
• gnomAD v3: 6-133546664-G-A
• gnomAD v4: 6-133546664-G-A
• MyVariant Identifiers: chr6:g.133867802G>A (hg19) ; chr6:g.133546664G>A (hg38)

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