Canonical Allele Identifier: CA2514845724
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50581966C>T , CM000684.2:g.50581966C>T GRCh38
NC_000022.10:g.51020395C>T , CM000684.1:g.51020395C>T GRCh37
NC_000022.9:g.49367261C>T NCBI36
NG_012643.1:g.1702G>A
NG_029213.1:g.6034G>A , LRG_855:g.6034G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.334-104G>A (CHKB) MANE Select ENSP00000384400.3:n.334-104G>A
ENST00000406938.2:c.334-104G>A (CHKB) ENSP00000384400.2:n.334-104G>A
ENST00000463053.1:n.482+63G>A (CHKB)
ENST00000465842.1:n.173-104G>A (CHKB)
ENST00000468532.5:n.211-104G>A (CHKB)
ENST00000476289.5:n.607-104G>A (CHKB)
ENST00000479003.5:n.855G>A (CHKB)
ENST00000481673.5:n.680G>A (CHKB)
ENST00000484266.5:n.576+283G>A (CHKB)
ENST00000492556.5:n.1000G>A (CHKB-CPT1B)
ENST00000492582.5:n.889G>A (CHKB)
NM_005198.4:c.334-104G>A , LRG_855t1:c.334-104G>A (CHKB) NP_005189.2:n.334-104G>A
NR_027928.2:n.552-104G>A (CHKB-CPT1B)
NM_005198.5:c.334-104G>A (CHKB) MANE Select NP_005189.2:n.334-104G>A