Canonical Allele Identifier: CA515274080

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50581446-G-C
• MyVariant Identifiers: chr22:g.51019875G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50581446G>C , CM000684.2:g.50581446G>C	GRCh38
NC_000022.10:g.51019875G>C , CM000684.1:g.51019875G>C	GRCh37
NC_000022.9:g.49366741G>C	NCBI36
NG_012643.1:g.2222C>G
NG_029213.1:g.6554C>G , LRG_855:g.6554C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.555C>G (CHKB) MANE Select	ENSP00000384400.3:p.Pro185=
ENST00000406938.2:c.555C>G (CHKB)	ENSP00000384400.2:p.Pro185=
ENST00000463053.1:n.704C>G (CHKB)
ENST00000468532.5:n.432C>G (CHKB)
ENST00000476289.5:n.828C>G (CHKB)
ENST00000479003.5:n.1180C>G (CHKB)
ENST00000481673.5:n.1005C>G (CHKB)
ENST00000484266.5:n.577-786C>G (CHKB)
ENST00000492556.5:n.1325C>G (CHKB-CPT1B)
ENST00000492582.5:n.1214C>G (CHKB)
NM_005198.4:c.555C>G , LRG_855t1:c.555C>G (CHKB)	NP_005189.2:p.Pro185=
NR_027928.2:n.773C>G (CHKB-CPT1B)
NM_005198.5:c.555C>G (CHKB) MANE Select	NP_005189.2:p.Pro185=