Canonical Allele Identifier: CA819231239

Gene: TARID

Linked Data

• dbSNP Id: rs1377319730
• gnomAD v3: 6-133875546-A-G
• gnomAD v4: 6-133875546-A-G
• MyVariant Identifiers: chr6:g.134196684A>G (hg19) ; chr6:g.133875546A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875546A>G , CM000668.2:g.133875546A>G	GRCh38
NC_000006.11:g.134196684A>G , CM000668.1:g.134196684A>G	GRCh37
NC_000006.10:g.134238377A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13058T>C