Canonical Allele Identifier: CA645372461
Gene: CNGB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 427721
ClinVar RCV Id: RCV000497920

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86577966_86582991del , CM000670.2:g.86577966_86582991del GRCh38
NC_000008.10:g.87590194_87595219del , CM000670.1:g.87590194_87595219del GRCh37
NC_000008.9:g.87659310_87664335del NCBI36
NG_016980.1:g.165701_170726del

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1782-3723_2103+739del
ENST00000681546.1:n.1602-3723_1923+739del
ENST00000681746.1:c.*193-3723_*514+739del
ENST00000320005.5:c.1782-3723_2103+739del
NM_019098.4:c.1782-3723_2103+739del
XM_011517138.1:c.1368-3723_1689+739del
XM_011517138.2:c.1368-3723_1689+739del
NM_019098.5:c.1782-3723_2103+739del