Canonical Allele Identifier: CA412202264

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs1257966850
• gnomAD v2: 22-51020692-C-T
• gnomAD v4: 22-50582263-C-T
• MyVariant Identifiers: chr22:g.51020692C>T (hg19) ; chr22:g.50582263C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582263C>T , CM000684.2:g.50582263C>T	GRCh38
NC_000022.10:g.51020692C>T , CM000684.1:g.51020692C>T	GRCh37
NC_000022.9:g.49367558C>T	NCBI36
NG_012643.1:g.1405G>A
NG_029213.1:g.5737G>A , LRG_855:g.5737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.319G>A (CHKB) MANE Select	ENSP00000384400.3:p.Gly107Arg
ENST00000406938.2:c.319G>A (CHKB)	ENSP00000384400.2:p.Gly107Arg
ENST00000463053.1:n.401G>A (CHKB)
ENST00000465842.1:n.158G>A (CHKB)
ENST00000468532.5:n.196G>A (CHKB)
ENST00000476289.5:n.592G>A (CHKB)
ENST00000479003.5:n.558G>A (CHKB)
ENST00000481673.5:n.383G>A (CHKB)
ENST00000484266.5:n.562G>A (CHKB)
ENST00000492556.5:n.703G>A (CHKB-CPT1B)
ENST00000492582.5:n.592G>A (CHKB)
NM_005198.4:c.319G>A , LRG_855t1:c.319G>A (CHKB)	NP_005189.2:p.Gly107Arg
NR_027928.2:n.537G>A (CHKB-CPT1B)
NM_005198.5:c.319G>A (CHKB) MANE Select	NP_005189.2:p.Gly107Arg