Canonical Allele Identifier: CA515274540
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51019980A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50581551A>G , CM000684.2:g.50581551A>G GRCh38
NC_000022.10:g.51019980A>G , CM000684.1:g.51019980A>G GRCh37
NC_000022.9:g.49366846A>G NCBI36
NG_012643.1:g.2117T>C
NG_029213.1:g.6449T>C , LRG_855:g.6449T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.450T>C (CHKB) MANE Select ENSP00000384400.3:p.Ser150=
ENST00000406938.2:c.450T>C (CHKB) ENSP00000384400.2:p.Ser150=
ENST00000463053.1:n.599T>C (CHKB)
ENST00000468532.5:n.327T>C (CHKB)
ENST00000476289.5:n.723T>C (CHKB)
ENST00000479003.5:n.1075T>C (CHKB)
ENST00000481673.5:n.900T>C (CHKB)
ENST00000484266.5:n.576+698T>C (CHKB)
ENST00000492556.5:n.1220T>C (CHKB-CPT1B)
ENST00000492582.5:n.1109T>C (CHKB)
NM_005198.4:c.450T>C , LRG_855t1:c.450T>C (CHKB) NP_005189.2:p.Ser150=
NR_027928.2:n.668T>C (CHKB-CPT1B)
NM_005198.5:c.450T>C (CHKB) MANE Select NP_005189.2:p.Ser150=