Canonical Allele Identifier: CA2577767396

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50581942-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50581942A>G , CM000684.2:g.50581942A>G	GRCh38
NC_000022.10:g.51020371A>G , CM000684.1:g.51020371A>G	GRCh37
NC_000022.9:g.49367237A>G	NCBI36
NG_012643.1:g.1726T>C
NG_029213.1:g.6058T>C , LRG_855:g.6058T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.334-80T>C (CHKB) MANE Select	ENSP00000384400.3:n.334-80T>C
ENST00000406938.2:c.334-80T>C (CHKB)	ENSP00000384400.2:n.334-80T>C
ENST00000463053.1:n.483-80T>C (CHKB)
ENST00000465842.1:n.173-80T>C (CHKB)
ENST00000468532.5:n.211-80T>C (CHKB)
ENST00000476289.5:n.607-80T>C (CHKB)
ENST00000479003.5:n.879T>C (CHKB)
ENST00000481673.5:n.704T>C (CHKB)
ENST00000484266.5:n.576+307T>C (CHKB)
ENST00000492556.5:n.1024T>C (CHKB-CPT1B)
ENST00000492582.5:n.913T>C (CHKB)
NM_005198.4:c.334-80T>C , LRG_855t1:c.334-80T>C (CHKB)	NP_005189.2:n.334-80T>C
NR_027928.2:n.552-80T>C (CHKB-CPT1B)
NM_005198.5:c.334-80T>C (CHKB) MANE Select	NP_005189.2:n.334-80T>C