Canonical Allele Identifier: CA612895408
Gene: TRAC HGNC NCBI

Linked Data

dbSNP Id: rs1182177932
gnomAD v2: 14-22999528-T-C
gnomAD v3: 14-22530577-T-C
gnomAD v4: 14-22530577-T-C
MyVariant Identifiers: chr14:g.22999528T>C (hg19) chr14:g.22530577T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22530577T>C , CM000676.2:g.22530577T>C GRCh38
NC_000014.8:g.22999528T>C , CM000676.1:g.22999528T>C GRCh37
NC_000014.7:g.22069368T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000616778.4:c.65-16929T>C ENSP00000482550.1:n.65-16929T>C
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