Canonical Allele Identifier: CA10323845

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs373182054
• ExAC: 22:51020807 C / T
• gnomAD v2: 22-51020807-C-T
• gnomAD v3: 22-50582378-C-T
• gnomAD v4: 22-50582378-C-T
• MyVariant Identifiers: chr22:g.51020807C>T (hg19) ; chr22:g.50582378C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582378C>T , CM000684.2:g.50582378C>T	GRCh38
NC_000022.10:g.51020807C>T , CM000684.1:g.51020807C>T	GRCh37
NC_000022.9:g.49367673C>T	NCBI36
NG_012643.1:g.1290G>A
NG_029213.1:g.5622G>A , LRG_855:g.5622G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.225-21G>A (CHKB) MANE Select	ENSP00000384400.3:n.225-21G>A
ENST00000406938.2:c.225-21G>A (CHKB)	ENSP00000384400.2:n.225-21G>A
ENST00000463053.1:n.307-21G>A (CHKB)
ENST00000465842.1:n.43G>A (CHKB)
ENST00000468532.5:n.81G>A (CHKB)
ENST00000476289.5:n.477G>A (CHKB)
ENST00000479003.5:n.443G>A (CHKB)
ENST00000481673.5:n.289-21G>A (CHKB)
ENST00000484266.5:n.447G>A (CHKB)
ENST00000492556.5:n.588G>A (CHKB-CPT1B)
ENST00000492582.5:n.477G>A (CHKB)
NM_005198.4:c.225-21G>A , LRG_855t1:c.225-21G>A (CHKB)	NP_005189.2:n.225-21G>A
NR_027928.2:n.443-21G>A (CHKB-CPT1B)
NM_005198.5:c.225-21G>A (CHKB) MANE Select	NP_005189.2:n.225-21G>A