Canonical Allele Identifier: CA412200373

Gene: CHKB CHKB-CPT1B

Linked Data

• MyVariant Identifiers: chr22:g.51019885G>C (hg19) ; chr22:g.50581456G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50581456G>C , CM000684.2:g.50581456G>C	GRCh38
NC_000022.10:g.51019885G>C , CM000684.1:g.51019885G>C	GRCh37
NC_000022.9:g.49366751G>C	NCBI36
NG_012643.1:g.2212C>G
NG_029213.1:g.6544C>G , LRG_855:g.6544C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.545C>G (CHKB) MANE Select	ENSP00000384400.3:p.Thr182Ser
ENST00000406938.2:c.545C>G (CHKB)	ENSP00000384400.2:p.Thr182Ser
ENST00000463053.1:n.694C>G (CHKB)
ENST00000468532.5:n.422C>G (CHKB)
ENST00000476289.5:n.818C>G (CHKB)
ENST00000479003.5:n.1170C>G (CHKB)
ENST00000481673.5:n.995C>G (CHKB)
ENST00000484266.5:n.576+793C>G (CHKB)
ENST00000492556.5:n.1315C>G (CHKB-CPT1B)
ENST00000492582.5:n.1204C>G (CHKB)
NM_005198.4:c.545C>G , LRG_855t1:c.545C>G (CHKB)	NP_005189.2:p.Thr182Ser
NR_027928.2:n.763C>G (CHKB-CPT1B)
NM_005198.5:c.545C>G (CHKB) MANE Select	NP_005189.2:p.Thr182Ser