Canonical Allele Identifier: CA515274518
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51019974T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50581545T>A , CM000684.2:g.50581545T>A GRCh38
NC_000022.10:g.51019974T>A , CM000684.1:g.51019974T>A GRCh37
NC_000022.9:g.49366840T>A NCBI36
NG_012643.1:g.2123A>T
NG_029213.1:g.6455A>T , LRG_855:g.6455A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.456A>T (CHKB) MANE Select ENSP00000384400.3:p.Pro152=
ENST00000406938.2:c.456A>T (CHKB) ENSP00000384400.2:p.Pro152=
ENST00000463053.1:n.605A>T (CHKB)
ENST00000468532.5:n.333A>T (CHKB)
ENST00000476289.5:n.729A>T (CHKB)
ENST00000479003.5:n.1081A>T (CHKB)
ENST00000481673.5:n.906A>T (CHKB)
ENST00000484266.5:n.576+704A>T (CHKB)
ENST00000492556.5:n.1226A>T (CHKB-CPT1B)
ENST00000492582.5:n.1115A>T (CHKB)
NM_005198.4:c.456A>T , LRG_855t1:c.456A>T (CHKB) NP_005189.2:p.Pro152=
NR_027928.2:n.674A>T (CHKB-CPT1B)
NM_005198.5:c.456A>T (CHKB) MANE Select NP_005189.2:p.Pro152=