Canonical Allele Identifier: CA371446346
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575992C>G , CM000670.2:g.86575992C>G GRCh38
NC_000008.10:g.87588220C>G , CM000670.1:g.87588220C>G GRCh37
NC_000008.9:g.87657336C>G NCBI36
NG_016980.1:g.172684G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.2242G>C MANE Select ENSP00000316605.5:p.Glu748Gln
ENST00000681546.1:n.2062G>C
ENST00000681746.1:c.*653G>C ENSP00000505959.1:n.*653G>C
ENST00000320005.5:c.2242G>C ENSP00000316605.5:p.Glu748Gln
ENST00000517327.5:c.276+2697G>C ENSP00000428329.1:n.276+2697G>C
NM_019098.4:c.2242G>C NP_061971.3:p.Glu748Gln
XM_011517138.1:c.1828G>C XP_011515440.1:p.Glu610Gln
XM_011517138.2:c.1828G>C XP_011515440.1:p.Glu610Gln
NM_019098.5:c.2242G>C MANE Select NP_061971.3:p.Glu748Gln