Canonical Allele Identifier: CA371446120
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575881T>G , CM000670.2:g.86575881T>G GRCh38
NC_000008.10:g.87588109T>G , CM000670.1:g.87588109T>G GRCh37
NC_000008.9:g.87657225T>G NCBI36
NG_016980.1:g.172795A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2353A>C MANE Select ENSP00000316605.5:p.Ile785Leu
ENST00000681546.1:n.2173A>C
ENST00000681746.1:c.*764A>C ENSP00000505959.1:n.*764A>C
ENST00000320005.5:c.2353A>C ENSP00000316605.5:p.Ile785Leu
ENST00000517327.5:c.276+2808A>C ENSP00000428329.1:n.276+2808A>C
NM_019098.4:c.2353A>C NP_061971.3:p.Ile785Leu
XM_011517138.1:c.1939A>C XP_011515440.1:p.Ile647Leu
XM_011517138.2:c.1939A>C XP_011515440.1:p.Ile647Leu
NM_019098.5:c.2353A>C MANE Select NP_061971.3:p.Ile785Leu