Canonical Allele Identifier: CA2616387440
Gene: CBL HGNC NCBI

Linked Data

dbSNP Id: rs2135303330

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119278094A>T , CM000673.2:g.119278094A>T GRCh38
NC_000011.9:g.119148804A>T , CM000673.1:g.119148804A>T GRCh37
NC_000011.8:g.118654014A>T NCBI36
NG_016808.1:g.76815A>T , LRG_608:g.76815A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700472.1:c.*548-72A>T ENSP00000515005.1:n.*548-72A>T
ENST00000264033.6:c.1096-72A>T MANE Select ENSP00000264033.3:n.1096-72A>T
ENST00000637974.1:c.1090-72A>T ENSP00000490763.1:n.1090-72A>T
ENST00000264033.5:c.1096-72A>T ENSP00000264033.3:n.1096-72A>T
ENST00000634586.1:c.1096-72A>T ENSP00000489218.1:n.1096-72A>T
ENST00000634840.1:c.1096-72A>T ENSP00000489324.1:n.1096-72A>T
NM_005188.3:c.1096-72A>T , LRG_608t1:c.1096-72A>T NP_005179.2:n.1096-72A>T
XM_011543057.1:c.1096-72A>T XP_011541359.1:n.1096-72A>T
NM_005188.4:c.1096-72A>T MANE Select NP_005179.2:n.1096-72A>T