Canonical Allele Identifier: CA15810353
Gene: TCL1A HGNC NCBI

Linked Data

dbSNP Id: rs7158782
gnomAD v2: 14-96169131-A-G
gnomAD v3: 14-95702794-A-G
gnomAD v4: 14-95702794-A-G
MyVariant Identifiers: chr14:g.96169131A>G (hg19) chr14:g.95702794A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95702794A>G , CM000676.2:g.95702794A>G GRCh38
NC_000014.8:g.96169131A>G , CM000676.1:g.96169131A>G GRCh37
NC_000014.7:g.95238884A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017021676.2:c.*2-8069T>C XP_016877165.1:n.*2-8069T>C
XM_017021677.2:c.*7-8069T>C XP_016877166.1:n.*7-8069T>C
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