Canonical Allele Identifier: CA754073345

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs1422325924
• gnomAD v3: 22-50582059-T-G
• gnomAD v4: 22-50582059-T-G
• MyVariant Identifiers: chr22:g.51020488T>G (hg19) ; chr22:g.50582059T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582059T>G , CM000684.2:g.50582059T>G	GRCh38
NC_000022.10:g.51020488T>G , CM000684.1:g.51020488T>G	GRCh37
NC_000022.9:g.49367354T>G	NCBI36
NG_012643.1:g.1609A>C
NG_029213.1:g.5941A>C , LRG_855:g.5941A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.333+190A>C (CHKB) MANE Select	ENSP00000384400.3:n.333+190A>C
ENST00000406938.2:c.333+190A>C (CHKB)	ENSP00000384400.2:n.333+190A>C
ENST00000463053.1:n.452A>C (CHKB)
ENST00000465842.1:n.172+190A>C (CHKB)
ENST00000468532.5:n.210+190A>C (CHKB)
ENST00000476289.5:n.606+190A>C (CHKB)
ENST00000479003.5:n.762A>C (CHKB)
ENST00000481673.5:n.587A>C (CHKB)
ENST00000484266.5:n.576+190A>C (CHKB)
ENST00000492556.5:n.907A>C (CHKB-CPT1B)
ENST00000492582.5:n.796A>C (CHKB)
NM_005198.4:c.333+190A>C , LRG_855t1:c.333+190A>C (CHKB)	NP_005189.2:n.333+190A>C
NR_027928.2:n.551+190A>C (CHKB-CPT1B)
NM_005198.5:c.333+190A>C (CHKB) MANE Select	NP_005189.2:n.333+190A>C