Canonical Allele Identifier: CA2724973589
Gene: CBL HGNC NCBI

Linked Data

dbSNP Id: rs1428738106

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278065A>T , CM000673.2:g.119278065A>T GRCh38
NC_000011.9:g.119148775A>T , CM000673.1:g.119148775A>T GRCh37
NC_000011.8:g.118653985A>T NCBI36
NG_016808.1:g.76786A>T , LRG_608:g.76786A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*548-101A>T ENSP00000515005.1:n.*548-101A>T
ENST00000264033.6:c.1096-101A>T MANE Select ENSP00000264033.3:n.1096-101A>T
ENST00000637974.1:c.1090-101A>T ENSP00000490763.1:n.1090-101A>T
ENST00000264033.5:c.1096-101A>T ENSP00000264033.3:n.1096-101A>T
ENST00000634586.1:c.1096-101A>T ENSP00000489218.1:n.1096-101A>T
ENST00000634840.1:c.1096-101A>T ENSP00000489324.1:n.1096-101A>T
NM_005188.3:c.1096-101A>T , LRG_608t1:c.1096-101A>T NP_005179.2:n.1096-101A>T
XM_011543057.1:c.1096-101A>T XP_011541359.1:n.1096-101A>T
NM_005188.4:c.1096-101A>T MANE Select NP_005179.2:n.1096-101A>T