Canonical Allele Identifier: CA1094686496

Gene: TARID

Linked Data

• gnomAD v3: 6-133875564-C-T
• gnomAD v4: 6-133875564-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875564C>T , CM000668.2:g.133875564C>T	GRCh38
NC_000006.11:g.134196702C>T , CM000668.1:g.134196702C>T	GRCh37
NC_000006.10:g.134238395C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13040G>A