Canonical Allele Identifier: CA10323631
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1111375
ClinVar RCV Id: RCV001437926
dbSNP Id: rs750764003

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50580198A>G , CM000684.2:g.50580198A>G GRCh38
NC_000022.10:g.51018627A>G , CM000684.1:g.51018627A>G GRCh37
NC_000022.9:g.49365493A>G NCBI36
NG_012643.1:g.3470T>C
NG_029213.1:g.7802T>C , LRG_855:g.7802T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000406938.3:c.810T>C (CHKB) MANE Select ENSP00000384400.3:p.Tyr270=
ENST00000406938.2:c.810T>C (CHKB) ENSP00000384400.2:p.Tyr270=
ENST00000464225.5:n.56T>C (CHKB)
ENST00000468532.5:n.773T>C (CHKB)
ENST00000471515.5:n.172T>C (CHKB)
ENST00000479003.5:n.1521T>C (CHKB)
ENST00000481673.5:n.1260T>C (CHKB)
ENST00000484266.5:n.805T>C (CHKB)
ENST00000489453.1:n.435T>C (CHKB)
ENST00000492556.5:n.1666T>C (CHKB-CPT1B)
ENST00000492582.5:n.1469T>C (CHKB)
NM_005198.4:c.810T>C , LRG_855t1:c.810T>C (CHKB) NP_005189.2:p.Tyr270=
NR_027928.2:n.1028T>C (CHKB-CPT1B)
NM_005198.5:c.810T>C (CHKB) MANE Select NP_005189.2:p.Tyr270=