Canonical Allele Identifier: CA2410936139

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs2070701313

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582008A>T , CM000684.2:g.50582008A>T	GRCh38
NC_000022.10:g.51020437A>T , CM000684.1:g.51020437A>T	GRCh37
NC_000022.9:g.49367303A>T	NCBI36
NG_012643.1:g.1660T>A
NG_029213.1:g.5992T>A , LRG_855:g.5992T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.334-146T>A (CHKB) MANE Select	ENSP00000384400.3:n.334-146T>A
ENST00000406938.2:c.334-146T>A (CHKB)	ENSP00000384400.2:n.334-146T>A
ENST00000463053.1:n.482+21T>A (CHKB)
ENST00000465842.1:n.173-146T>A (CHKB)
ENST00000468532.5:n.211-146T>A (CHKB)
ENST00000476289.5:n.607-146T>A (CHKB)
ENST00000479003.5:n.813T>A (CHKB)
ENST00000481673.5:n.638T>A (CHKB)
ENST00000484266.5:n.576+241T>A (CHKB)
ENST00000492556.5:n.958T>A (CHKB-CPT1B)
ENST00000492582.5:n.847T>A (CHKB)
NM_005198.4:c.334-146T>A , LRG_855t1:c.334-146T>A (CHKB)	NP_005189.2:n.334-146T>A
NR_027928.2:n.552-146T>A (CHKB-CPT1B)
NM_005198.5:c.334-146T>A (CHKB) MANE Select	NP_005189.2:n.334-146T>A