Canonical Allele Identifier: CA2657583976

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50581964-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50581964G>T , CM000684.2:g.50581964G>T	GRCh38
NC_000022.10:g.51020393G>T , CM000684.1:g.51020393G>T	GRCh37
NC_000022.9:g.49367259G>T	NCBI36
NG_012643.1:g.1704C>A
NG_029213.1:g.6036C>A , LRG_855:g.6036C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.334-102C>A (CHKB) MANE Select	ENSP00000384400.3:n.334-102C>A
ENST00000406938.2:c.334-102C>A (CHKB)	ENSP00000384400.2:n.334-102C>A
ENST00000463053.1:n.482+65C>A (CHKB)
ENST00000465842.1:n.173-102C>A (CHKB)
ENST00000468532.5:n.211-102C>A (CHKB)
ENST00000476289.5:n.607-102C>A (CHKB)
ENST00000479003.5:n.857C>A (CHKB)
ENST00000481673.5:n.682C>A (CHKB)
ENST00000484266.5:n.576+285C>A (CHKB)
ENST00000492556.5:n.1002C>A (CHKB-CPT1B)
ENST00000492582.5:n.891C>A (CHKB)
NM_005198.4:c.334-102C>A , LRG_855t1:c.334-102C>A (CHKB)	NP_005189.2:n.334-102C>A
NR_027928.2:n.552-102C>A (CHKB-CPT1B)
NM_005198.5:c.334-102C>A (CHKB) MANE Select	NP_005189.2:n.334-102C>A