Canonical Allele Identifier: CA144693

Gene: TRAC

Linked Data

• ClinVar Variation Id: 64370
• ClinVar RCV Id: RCV000054556
• dbSNP Id: rs397514259
• MyVariant Identifiers: chr14:g.23019608G>A (hg19) ; chr14:g.22550664G>A (hg38)
• PubMed: PMID:21206088

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22550664G>A , CM000676.2:g.22550664G>A	GRCh38
NC_000014.8:g.23019608G>A , CM000676.1:g.23019608G>A	GRCh37
NC_000014.7:g.22089448G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000611116.2:c.426G>A
ENST00000611116.1:c.426G>A
ENST00000616778.4:c.*1G>A	ENSP00000482550.1:n.*1G>A