Canonical Allele Identifier: CA412202892

Gene: CHKB CHKB-CPT1B

Linked Data

• MyVariant Identifiers: chr22:g.51020986C>A (hg19) ; chr22:g.50582557C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582557C>A , CM000684.2:g.50582557C>A	GRCh38
NC_000022.10:g.51020986C>A , CM000684.1:g.51020986C>A	GRCh37
NC_000022.9:g.49367852C>A	NCBI36
NG_012643.1:g.1111G>T
NG_029213.1:g.5443G>T , LRG_855:g.5443G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.224+1G>T (CHKB) MANE Select	ENSP00000384400.3:n.224+1G>T
ENST00000406938.2:c.224+1G>T (CHKB)	ENSP00000384400.2:n.224+1G>T
ENST00000463053.1:n.307-200G>T (CHKB)
ENST00000476289.5:n.298G>T (CHKB)
ENST00000479003.5:n.264G>T (CHKB)
ENST00000481673.5:n.288+1G>T (CHKB)
ENST00000484266.5:n.268G>T (CHKB)
ENST00000492556.5:n.409G>T (CHKB-CPT1B)
ENST00000492582.5:n.298G>T (CHKB)
NM_005198.4:c.224+1G>T , LRG_855t1:c.224+1G>T (CHKB)	NP_005189.2:n.224+1G>T
NR_027928.2:n.442+1G>T (CHKB-CPT1B)
NM_005198.5:c.224+1G>T (CHKB) MANE Select	NP_005189.2:n.224+1G>T