Canonical Allele Identifier: CA640055269

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs1308986637
• gnomAD v2: 22-51020358-T-G
• gnomAD v3: 22-50581929-T-G
• gnomAD v4: 22-50581929-T-G
• MyVariant Identifiers: chr22:g.51020358T>G (hg19) ; chr22:g.50581929T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50581929T>G , CM000684.2:g.50581929T>G	GRCh38
NC_000022.10:g.51020358T>G , CM000684.1:g.51020358T>G	GRCh37
NC_000022.9:g.49367224T>G	NCBI36
NG_012643.1:g.1739A>C
NG_029213.1:g.6071A>C , LRG_855:g.6071A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.334-67A>C (CHKB) MANE Select	ENSP00000384400.3:n.334-67A>C
ENST00000406938.2:c.334-67A>C (CHKB)	ENSP00000384400.2:n.334-67A>C
ENST00000463053.1:n.483-67A>C (CHKB)
ENST00000465842.1:n.173-67A>C (CHKB)
ENST00000468532.5:n.211-67A>C (CHKB)
ENST00000476289.5:n.607-67A>C (CHKB)
ENST00000479003.5:n.892A>C (CHKB)
ENST00000481673.5:n.717A>C (CHKB)
ENST00000484266.5:n.576+320A>C (CHKB)
ENST00000492556.5:n.1037A>C (CHKB-CPT1B)
ENST00000492582.5:n.926A>C (CHKB)
NM_005198.4:c.334-67A>C , LRG_855t1:c.334-67A>C (CHKB)	NP_005189.2:n.334-67A>C
NR_027928.2:n.552-67A>C (CHKB-CPT1B)
NM_005198.5:c.334-67A>C (CHKB) MANE Select	NP_005189.2:n.334-67A>C