Canonical Allele Identifier: CA412200465
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51019899C>A (hg19) chr22:g.50581470C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50581470C>A , CM000684.2:g.50581470C>A GRCh38
NC_000022.10:g.51019899C>A , CM000684.1:g.51019899C>A GRCh37
NC_000022.9:g.49366765C>A NCBI36
NG_012643.1:g.2198G>T
NG_029213.1:g.6530G>T , LRG_855:g.6530G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.531G>T (CHKB) MANE Select ENSP00000384400.3:p.Met177Ile
ENST00000406938.2:c.531G>T (CHKB) ENSP00000384400.2:p.Met177Ile
ENST00000463053.1:n.680G>T (CHKB)
ENST00000468532.5:n.408G>T (CHKB)
ENST00000476289.5:n.804G>T (CHKB)
ENST00000479003.5:n.1156G>T (CHKB)
ENST00000481673.5:n.981G>T (CHKB)
ENST00000484266.5:n.576+779G>T (CHKB)
ENST00000492556.5:n.1301G>T (CHKB-CPT1B)
ENST00000492582.5:n.1190G>T (CHKB)
NM_005198.4:c.531G>T , LRG_855t1:c.531G>T (CHKB) NP_005189.2:p.Met177Ile
NR_027928.2:n.749G>T (CHKB-CPT1B)
NM_005198.5:c.531G>T (CHKB) MANE Select NP_005189.2:p.Met177Ile
Search 100 bp 5'
Search 100 bp 3'