Canonical Allele Identifier: CA2838385097
Gene: TARID HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133671013A>T , CM000668.2:g.133671013A>T GRCh38
NC_000006.11:g.133992151A>T , CM000668.1:g.133992151A>T GRCh37
NC_000006.10:g.134033844A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109982.1:n.647+89172T>A
Search 100 bp 5'
Search 100 bp 3'