Canonical Allele Identifier: CA2657584018

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50582013-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582013G>A , CM000684.2:g.50582013G>A	GRCh38
NC_000022.10:g.51020442G>A , CM000684.1:g.51020442G>A	GRCh37
NC_000022.9:g.49367308G>A	NCBI36
NG_012643.1:g.1655C>T
NG_029213.1:g.5987C>T , LRG_855:g.5987C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.334-151C>T (CHKB) MANE Select	ENSP00000384400.3:n.334-151C>T
ENST00000406938.2:c.334-151C>T (CHKB)	ENSP00000384400.2:n.334-151C>T
ENST00000463053.1:n.482+16C>T (CHKB)
ENST00000465842.1:n.173-151C>T (CHKB)
ENST00000468532.5:n.211-151C>T (CHKB)
ENST00000476289.5:n.607-151C>T (CHKB)
ENST00000479003.5:n.808C>T (CHKB)
ENST00000481673.5:n.633C>T (CHKB)
ENST00000484266.5:n.576+236C>T (CHKB)
ENST00000492556.5:n.953C>T (CHKB-CPT1B)
ENST00000492582.5:n.842C>T (CHKB)
NM_005198.4:c.334-151C>T , LRG_855t1:c.334-151C>T (CHKB)	NP_005189.2:n.334-151C>T
NR_027928.2:n.552-151C>T (CHKB-CPT1B)
NM_005198.5:c.334-151C>T (CHKB) MANE Select	NP_005189.2:n.334-151C>T