Canonical Allele Identifier: CA819231255

Gene: TARID

Linked Data

• dbSNP Id: rs899751081
• gnomAD v3: 6-133875589-T-TA
• gnomAD v4: 6-133875589-T-TA
• MyVariant Identifiers: chr6:g.134196727_134196728insA (hg19) ; chr6:g.133875589_133875590insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875597dup , CM000668.2:g.133875597dup	GRCh38
NC_000006.11:g.134196735dup , CM000668.1:g.134196735dup	GRCh37
NC_000006.10:g.134238428dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13014dup