Canonical Allele Identifier: CA819231229

Gene: TARID

Linked Data

• dbSNP Id: rs1430744717
• MyVariant Identifiers: chr6:g.134196675G>T (hg19) ; chr6:g.133875537G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875537G>T , CM000668.2:g.133875537G>T	GRCh38
NC_000006.11:g.134196675G>T , CM000668.1:g.134196675G>T	GRCh37
NC_000006.10:g.134238368G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13067C>A