Canonical Allele Identifier: CA371446116
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575880A>C , CM000670.2:g.86575880A>C GRCh38
NC_000008.10:g.87588108A>C , CM000670.1:g.87588108A>C GRCh37
NC_000008.9:g.87657224A>C NCBI36
NG_016980.1:g.172796T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2354T>G MANE Select ENSP00000316605.5:p.Ile785Ser
ENST00000681546.1:n.2174T>G
ENST00000681746.1:c.*765T>G ENSP00000505959.1:n.*765T>G
ENST00000320005.5:c.2354T>G ENSP00000316605.5:p.Ile785Ser
ENST00000517327.5:c.276+2809T>G ENSP00000428329.1:n.276+2809T>G
NM_019098.4:c.2354T>G NP_061971.3:p.Ile785Ser
XM_011517138.1:c.1940T>G XP_011515440.1:p.Ile647Ser
XM_011517138.2:c.1940T>G XP_011515440.1:p.Ile647Ser
NM_019098.5:c.2354T>G MANE Select NP_061971.3:p.Ile785Ser