Canonical Allele Identifier: CA2657584522
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50582454C>A , CM000684.2:g.50582454C>A GRCh38
NC_000022.10:g.51020883C>A , CM000684.1:g.51020883C>A GRCh37
NC_000022.9:g.49367749C>A NCBI36
NG_012643.1:g.1214G>T
NG_029213.1:g.5546G>T , LRG_855:g.5546G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.225-97G>T (CHKB) MANE Select ENSP00000384400.3:n.225-97G>T
ENST00000406938.2:c.225-97G>T (CHKB) ENSP00000384400.2:n.225-97G>T
ENST00000463053.1:n.307-97G>T (CHKB)
ENST00000468532.5:n.5G>T (CHKB)
ENST00000476289.5:n.401G>T (CHKB)
ENST00000479003.5:n.367G>T (CHKB)
ENST00000481673.5:n.289-97G>T (CHKB)
ENST00000484266.5:n.371G>T (CHKB)
ENST00000492556.5:n.512G>T (CHKB-CPT1B)
ENST00000492582.5:n.401G>T (CHKB)
NM_005198.4:c.225-97G>T , LRG_855t1:c.225-97G>T (CHKB) NP_005189.2:n.225-97G>T
NR_027928.2:n.443-97G>T (CHKB-CPT1B)
NM_005198.5:c.225-97G>T (CHKB) MANE Select NP_005189.2:n.225-97G>T