Canonical Allele Identifier: CA7334427
Gene: TCL1B HGNC NCBI
COSMIC:
COSM1371885 (not active)
MyVariant.info:
GRCh38 chr14:g.95690850G>A
GRCh37 chr14:g.96157187G>A
Revel Score:
ENST00000340722 (MANE Select) 0.071
ENST00000538038 0.071
gnomAD v2:
14:96157187 G / A
gnomAD v3:
14:95690850 G / A
gnomAD v4:
chr14-95690850-G-A
Joint Max Group AF 0.45120245 (NFE)
Genomes Max Group AF 0.44555773 (NFE)
Exomes Max Group AF 0.45132044 (NFE)
dbSNP:
1064017
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000340722.8:c.277G>A MANE Select ENSP00000343223.6:p.Gly93Arg
ENST00000340722.7:c.277G>A ENSP00000343223.6:p.Gly93Arg
ENST00000464815.5:n.307G>A
ENST00000556665.1:n.237G>A
NM_004918.3:c.277G>A NP_004909.1:p.Gly93Arg
NM_004918.4:c.277G>A MANE Select NP_004909.1:p.Gly93Arg
Search 100 bp 5'
Search 100 bp 3'