Canonical Allele Identifier: CA148431576

Gene: TARID

Linked Data

• dbSNP Id: rs899751081
• gnomAD v2: 6-134196727-TA-T
• gnomAD v3: 6-133875589-TA-T
• gnomAD v4: 6-133875589-TA-T
• MyVariant Identifiers: chr6:g.134196728del (hg19) ; chr6:g.133875590del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133875597del , CM000668.2:g.133875597del	GRCh38
NC_000006.11:g.134196735del , CM000668.1:g.134196735del	GRCh37
NC_000006.10:g.134238428del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109982.1:n.403+13014del