Canonical Allele Identifier: CA515275823

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50582330-G-T
• MyVariant Identifiers: chr22:g.51020759G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582330G>T , CM000684.2:g.50582330G>T	GRCh38
NC_000022.10:g.51020759G>T , CM000684.1:g.51020759G>T	GRCh37
NC_000022.9:g.49367625G>T	NCBI36
NG_012643.1:g.1338C>A
NG_029213.1:g.5670C>A , LRG_855:g.5670C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.252C>A (CHKB) MANE Select	ENSP00000384400.3:p.Arg84=
ENST00000406938.2:c.252C>A (CHKB)	ENSP00000384400.2:p.Arg84=
ENST00000463053.1:n.334C>A (CHKB)
ENST00000465842.1:n.91C>A (CHKB)
ENST00000468532.5:n.129C>A (CHKB)
ENST00000476289.5:n.525C>A (CHKB)
ENST00000479003.5:n.491C>A (CHKB)
ENST00000481673.5:n.316C>A (CHKB)
ENST00000484266.5:n.495C>A (CHKB)
ENST00000492556.5:n.636C>A (CHKB-CPT1B)
ENST00000492582.5:n.525C>A (CHKB)
NM_005198.4:c.252C>A , LRG_855t1:c.252C>A (CHKB)	NP_005189.2:p.Arg84=
NR_027928.2:n.470C>A (CHKB-CPT1B)
NM_005198.5:c.252C>A (CHKB) MANE Select	NP_005189.2:p.Arg84=