ClinGen Allele Registry
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Canonical Allele Identifier:
CA704227493
Gene: TRAC
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.22533736G>A
Linked Data - NCBI & NCI
dbSNP:
1154155
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.22533736G>A , CM000676.2:g.22533736G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000616778.4:c.65-13770G>A
ENSP00000482550.1:n.65-13770G>A
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