Canonical Allele Identifier: CA371446327
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575983G>T , CM000670.2:g.86575983G>T GRCh38
NC_000008.10:g.87588211G>T , CM000670.1:g.87588211G>T GRCh37
NC_000008.9:g.87657327G>T NCBI36
NG_016980.1:g.172693C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2251C>A MANE Select ENSP00000316605.5:p.Leu751Met
ENST00000681546.1:n.2071C>A
ENST00000681746.1:c.*662C>A ENSP00000505959.1:n.*662C>A
ENST00000320005.5:c.2251C>A ENSP00000316605.5:p.Leu751Met
ENST00000517327.5:c.276+2706C>A ENSP00000428329.1:n.276+2706C>A
NM_019098.4:c.2251C>A NP_061971.3:p.Leu751Met
XM_011517138.1:c.1837C>A XP_011515440.1:p.Leu613Met
XM_011517138.2:c.1837C>A XP_011515440.1:p.Leu613Met
NM_019098.5:c.2251C>A MANE Select NP_061971.3:p.Leu751Met