Canonical Allele Identifier: CA257664559
Gene: TRAC HGNC NCBI
MyVariant.info:
GRCh38 chr14:g.22533736G>T
gnomAD v3:
14:22533736 G / T
gnomAD v4:
chr14-22533736-G-T
Joint Max Group AF 0.93479031 (AFR)
Genomes Max Group AF 0.93479031 (AFR)
dbSNP:
1154155
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22533736G>T , CM000676.2:g.22533736G>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000616778.4:c.65-13770G>T ENSP00000482550.1:n.65-13770G>T
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