Canonical Allele Identifier: CA640358348

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs1269650065
• gnomAD v2: 22-51020865-G-A
• gnomAD v4: 22-50582436-G-A
• MyVariant Identifiers: chr22:g.51020865G>A (hg19) ; chr22:g.50582436G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582436G>A , CM000684.2:g.50582436G>A	GRCh38
NC_000022.10:g.51020865G>A , CM000684.1:g.51020865G>A	GRCh37
NC_000022.9:g.49367731G>A	NCBI36
NG_012643.1:g.1232C>T
NG_029213.1:g.5564C>T , LRG_855:g.5564C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.225-79C>T (CHKB) MANE Select	ENSP00000384400.3:n.225-79C>T
ENST00000406938.2:c.225-79C>T (CHKB)	ENSP00000384400.2:n.225-79C>T
ENST00000463053.1:n.307-79C>T (CHKB)
ENST00000468532.5:n.23C>T (CHKB)
ENST00000476289.5:n.419C>T (CHKB)
ENST00000479003.5:n.385C>T (CHKB)
ENST00000481673.5:n.289-79C>T (CHKB)
ENST00000484266.5:n.389C>T (CHKB)
ENST00000492556.5:n.530C>T (CHKB-CPT1B)
ENST00000492582.5:n.419C>T (CHKB)
NM_005198.4:c.225-79C>T , LRG_855t1:c.225-79C>T (CHKB)	NP_005189.2:n.225-79C>T
NR_027928.2:n.443-79C>T (CHKB-CPT1B)
NM_005198.5:c.225-79C>T (CHKB) MANE Select	NP_005189.2:n.225-79C>T