Canonical Allele Identifier: CA2410936498
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

dbSNP Id: rs2070719712

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50582529A>C , CM000684.2:g.50582529A>C GRCh38
NC_000022.10:g.51020958A>C , CM000684.1:g.51020958A>C GRCh37
NC_000022.9:g.49367824A>C NCBI36
NG_012643.1:g.1139T>G
NG_029213.1:g.5471T>G , LRG_855:g.5471T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.224+29T>G (CHKB) MANE Select ENSP00000384400.3:n.224+29T>G
ENST00000406938.2:c.224+29T>G (CHKB) ENSP00000384400.2:n.224+29T>G
ENST00000463053.1:n.307-172T>G (CHKB)
ENST00000476289.5:n.326T>G (CHKB)
ENST00000479003.5:n.292T>G (CHKB)
ENST00000481673.5:n.288+29T>G (CHKB)
ENST00000484266.5:n.296T>G (CHKB)
ENST00000492556.5:n.437T>G (CHKB-CPT1B)
ENST00000492582.5:n.326T>G (CHKB)
NM_005198.4:c.224+29T>G , LRG_855t1:c.224+29T>G (CHKB) NP_005189.2:n.224+29T>G
NR_027928.2:n.442+29T>G (CHKB-CPT1B)
NM_005198.5:c.224+29T>G (CHKB) MANE Select NP_005189.2:n.224+29T>G