Canonical Allele Identifier: CA412200279
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51019862C>A (hg19) chr22:g.50581433C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50581433C>A , CM000684.2:g.50581433C>A GRCh38
NC_000022.10:g.51019862C>A , CM000684.1:g.51019862C>A GRCh37
NC_000022.9:g.49366728C>A NCBI36
NG_012643.1:g.2235G>T
NG_029213.1:g.6567G>T , LRG_855:g.6567G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.568G>T (CHKB) MANE Select ENSP00000384400.3:p.Gly190Trp
ENST00000406938.2:c.568G>T (CHKB) ENSP00000384400.2:p.Gly190Trp
ENST00000463053.1:n.717G>T (CHKB)
ENST00000468532.5:n.445G>T (CHKB)
ENST00000476289.5:n.841G>T (CHKB)
ENST00000479003.5:n.1193G>T (CHKB)
ENST00000481673.5:n.1018G>T (CHKB)
ENST00000484266.5:n.577-773G>T (CHKB)
ENST00000492556.5:n.1338G>T (CHKB-CPT1B)
ENST00000492582.5:n.1227G>T (CHKB)
NM_005198.4:c.568G>T , LRG_855t1:c.568G>T (CHKB) NP_005189.2:p.Gly190Trp
NR_027928.2:n.786G>T (CHKB-CPT1B)
NM_005198.5:c.568G>T (CHKB) MANE Select NP_005189.2:p.Gly190Trp
Search 100 bp 5'
Search 100 bp 3'