Canonical Allele Identifier: CA2819320588
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50582419C>G , CM000684.2:g.50582419C>G GRCh38
NC_000022.10:g.51020848C>G , CM000684.1:g.51020848C>G GRCh37
NC_000022.9:g.49367714C>G NCBI36
NG_012643.1:g.1249G>C
NG_029213.1:g.5581G>C , LRG_855:g.5581G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.225-62G>C (CHKB) MANE Select ENSP00000384400.3:n.225-62G>C
ENST00000406938.2:c.225-62G>C (CHKB) ENSP00000384400.2:n.225-62G>C
ENST00000463053.1:n.307-62G>C (CHKB)
ENST00000465842.1:n.2G>C (CHKB)
ENST00000468532.5:n.40G>C (CHKB)
ENST00000476289.5:n.436G>C (CHKB)
ENST00000479003.5:n.402G>C (CHKB)
ENST00000481673.5:n.289-62G>C (CHKB)
ENST00000484266.5:n.406G>C (CHKB)
ENST00000492556.5:n.547G>C (CHKB-CPT1B)
ENST00000492582.5:n.436G>C (CHKB)
NM_005198.4:c.225-62G>C , LRG_855t1:c.225-62G>C (CHKB) NP_005189.2:n.225-62G>C
NR_027928.2:n.443-62G>C (CHKB-CPT1B)
NM_005198.5:c.225-62G>C (CHKB) MANE Select NP_005189.2:n.225-62G>C