Canonical Allele Identifier: CA1094686509

Gene: TARID

Linked Data

• dbSNP Id: rs1774970460
• gnomAD v3: 6-133875601-T-C
• gnomAD v4: 6-133875601-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875601T>C , CM000668.2:g.133875601T>C	GRCh38
NC_000006.11:g.134196739T>C , CM000668.1:g.134196739T>C	GRCh37
NC_000006.10:g.134238432T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13003A>G