Canonical Allele Identifier: CA570671261

Gene: TARID

Linked Data

• dbSNP Id: rs1242323656
• gnomAD v2: 6-134196621-G-A
• gnomAD v3: 6-133875483-G-A
• gnomAD v4: 6-133875483-G-A
• MyVariant Identifiers: chr6:g.134196621G>A (hg19) ; chr6:g.133875483G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875483G>A , CM000668.2:g.133875483G>A	GRCh38
NC_000006.11:g.134196621G>A , CM000668.1:g.134196621G>A	GRCh37
NC_000006.10:g.134238314G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_109982.1:n.403+13121C>T