Canonical Allele Identifier: CA412202752

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs1284727525
• gnomAD v2: 22-51020785-C-A
• gnomAD v4: 22-50582356-C-A
• MyVariant Identifiers: chr22:g.51020785C>A (hg19) ; chr22:g.50582356C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582356C>A , CM000684.2:g.50582356C>A	GRCh38
NC_000022.10:g.51020785C>A , CM000684.1:g.51020785C>A	GRCh37
NC_000022.9:g.49367651C>A	NCBI36
NG_012643.1:g.1312G>T
NG_029213.1:g.5644G>T , LRG_855:g.5644G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.226G>T (CHKB) MANE Select	ENSP00000384400.3:p.Gly76Ter
ENST00000406938.2:c.226G>T (CHKB)	ENSP00000384400.2:p.Gly76Ter
ENST00000463053.1:n.308G>T (CHKB)
ENST00000465842.1:n.65G>T (CHKB)
ENST00000468532.5:n.103G>T (CHKB)
ENST00000476289.5:n.499G>T (CHKB)
ENST00000479003.5:n.465G>T (CHKB)
ENST00000481673.5:n.290G>T (CHKB)
ENST00000484266.5:n.469G>T (CHKB)
ENST00000492556.5:n.610G>T (CHKB-CPT1B)
ENST00000492582.5:n.499G>T (CHKB)
NM_005198.4:c.226G>T , LRG_855t1:c.226G>T (CHKB)	NP_005189.2:p.Gly76Ter
NR_027928.2:n.444G>T (CHKB-CPT1B)
NM_005198.5:c.226G>T (CHKB) MANE Select	NP_005189.2:p.Gly76Ter