Canonical Allele Identifier: CA515274381
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51019947T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50581518T>A , CM000684.2:g.50581518T>A GRCh38
NC_000022.10:g.51019947T>A , CM000684.1:g.51019947T>A GRCh37
NC_000022.9:g.49366813T>A NCBI36
NG_012643.1:g.2150A>T
NG_029213.1:g.6482A>T , LRG_855:g.6482A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.483A>T (CHKB) MANE Select ENSP00000384400.3:p.Pro161=
ENST00000406938.2:c.483A>T (CHKB) ENSP00000384400.2:p.Pro161=
ENST00000463053.1:n.632A>T (CHKB)
ENST00000468532.5:n.360A>T (CHKB)
ENST00000476289.5:n.756A>T (CHKB)
ENST00000479003.5:n.1108A>T (CHKB)
ENST00000481673.5:n.933A>T (CHKB)
ENST00000484266.5:n.576+731A>T (CHKB)
ENST00000492556.5:n.1253A>T (CHKB-CPT1B)
ENST00000492582.5:n.1142A>T (CHKB)
NM_005198.4:c.483A>T , LRG_855t1:c.483A>T (CHKB) NP_005189.2:p.Pro161=
NR_027928.2:n.701A>T (CHKB-CPT1B)
NM_005198.5:c.483A>T (CHKB) MANE Select NP_005189.2:p.Pro161=