Canonical Allele Identifier: CA570671276

Gene: TARID

Linked Data

• dbSNP Id: rs1470018570
• gnomAD v2: 6-134196718-T-C
• gnomAD v3: 6-133875580-T-C
• gnomAD v4: 6-133875580-T-C
• MyVariant Identifiers: chr6:g.134196718T>C (hg19) ; chr6:g.133875580T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875580T>C , CM000668.2:g.133875580T>C	GRCh38
NC_000006.11:g.134196718T>C , CM000668.1:g.134196718T>C	GRCh37
NC_000006.10:g.134238411T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13024A>G