Canonical Allele Identifier: CA515275852
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51020998A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50582569A>T , CM000684.2:g.50582569A>T GRCh38
NC_000022.10:g.51020998A>T , CM000684.1:g.51020998A>T GRCh37
NC_000022.9:g.49367864A>T NCBI36
NG_012643.1:g.1099T>A
NG_029213.1:g.5431T>A , LRG_855:g.5431T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.213T>A (CHKB) MANE Select ENSP00000384400.3:p.Val71=
ENST00000406938.2:c.213T>A (CHKB) ENSP00000384400.2:p.Val71=
ENST00000463053.1:n.307-212T>A (CHKB)
ENST00000476289.5:n.286T>A (CHKB)
ENST00000479003.5:n.252T>A (CHKB)
ENST00000481673.5:n.277T>A (CHKB)
ENST00000484266.5:n.256T>A (CHKB)
ENST00000492556.5:n.397T>A (CHKB-CPT1B)
ENST00000492582.5:n.286T>A (CHKB)
NM_005198.4:c.213T>A , LRG_855t1:c.213T>A (CHKB) NP_005189.2:p.Val71=
NR_027928.2:n.431T>A (CHKB-CPT1B)
NM_005198.5:c.213T>A (CHKB) MANE Select NP_005189.2:p.Val71=