Canonical Allele Identifier: CA515273987

Gene: CHKB CHKB-CPT1B

Linked Data

• dbSNP Id: rs201476966
• gnomAD v2: 22-51019857-G-A
• gnomAD v4: 22-50581428-G-A
• MyVariant Identifiers: chr22:g.51019857G>A (hg19) ; chr22:g.50581428G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50581428G>A , CM000684.2:g.50581428G>A	GRCh38
NC_000022.10:g.51019857G>A , CM000684.1:g.51019857G>A	GRCh37
NC_000022.9:g.49366723G>A	NCBI36
NG_012643.1:g.2240C>T
NG_029213.1:g.6572C>T , LRG_855:g.6572C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.573C>T (CHKB) MANE Select	ENSP00000384400.3:p.Thr191=
ENST00000406938.2:c.573C>T (CHKB)	ENSP00000384400.2:p.Thr191=
ENST00000463053.1:n.722C>T (CHKB)
ENST00000468532.5:n.450C>T (CHKB)
ENST00000476289.5:n.846C>T (CHKB)
ENST00000479003.5:n.1198C>T (CHKB)
ENST00000481673.5:n.1023C>T (CHKB)
ENST00000484266.5:n.577-768C>T (CHKB)
ENST00000492556.5:n.1343C>T (CHKB-CPT1B)
ENST00000492582.5:n.1232C>T (CHKB)
NM_005198.4:c.573C>T , LRG_855t1:c.573C>T (CHKB)	NP_005189.2:p.Thr191=
NR_027928.2:n.791C>T (CHKB-CPT1B)
NM_005198.5:c.573C>T (CHKB) MANE Select	NP_005189.2:p.Thr191=