Canonical Allele Identifier: CA390897745
Gene: TCL1B HGNC NCBI
MyVariant.info:
GRCh38 chr14:g.95690850G>T
GRCh37 chr14:g.96157187G>T
Revel Score:
ENST00000340722 (MANE Select) 0.083
ENST00000538038 0.083
gnomAD v2:
14:96157187 G / T
gnomAD v4:
chr14-95690850-G-T
Joint Max Group AF 6.8e-7 (NFE)
Exomes Max Group AF 7.2e-7 (NFE)
dbSNP:
1064017
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.95690850G>T , CM000676.2:g.95690850G>T GRCh38
NC_000014.8:g.96157187G>T , CM000676.1:g.96157187G>T GRCh37
NC_000014.7:g.95226940G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000340722.8:c.277G>T MANE Select ENSP00000343223.6:p.Gly93Trp
ENST00000340722.7:c.277G>T ENSP00000343223.6:p.Gly93Trp
ENST00000464815.5:n.307G>T
ENST00000556665.1:n.237G>T
NM_004918.3:c.277G>T NP_004909.1:p.Gly93Trp
NM_004918.4:c.277G>T MANE Select NP_004909.1:p.Gly93Trp
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