Canonical Allele Identifier: CA515275782

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs1383925459
• gnomAD v2: 22-51020717-G-A
• gnomAD v4: 22-50582288-G-A
• MyVariant Identifiers: chr22:g.51020717G>A (hg19) ; chr22:g.50582288G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582288G>A , CM000684.2:g.50582288G>A	GRCh38
NC_000022.10:g.51020717G>A , CM000684.1:g.51020717G>A	GRCh37
NC_000022.9:g.49367583G>A	NCBI36
NG_012643.1:g.1380C>T
NG_029213.1:g.5712C>T , LRG_855:g.5712C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.294C>T (CHKB) MANE Select	ENSP00000384400.3:p.Pro98=
ENST00000406938.2:c.294C>T (CHKB)	ENSP00000384400.2:p.Pro98=
ENST00000463053.1:n.376C>T (CHKB)
ENST00000465842.1:n.133C>T (CHKB)
ENST00000468532.5:n.171C>T (CHKB)
ENST00000476289.5:n.567C>T (CHKB)
ENST00000479003.5:n.533C>T (CHKB)
ENST00000481673.5:n.358C>T (CHKB)
ENST00000484266.5:n.537C>T (CHKB)
ENST00000492556.5:n.678C>T (CHKB-CPT1B)
ENST00000492582.5:n.567C>T (CHKB)
NM_005198.4:c.294C>T , LRG_855t1:c.294C>T (CHKB)	NP_005189.2:p.Pro98=
NR_027928.2:n.512C>T (CHKB-CPT1B)
NM_005198.5:c.294C>T (CHKB) MANE Select	NP_005189.2:p.Pro98=