Canonical Allele Identifier: CA371446105
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575875T>A , CM000670.2:g.86575875T>A GRCh38
NC_000008.10:g.87588103T>A , CM000670.1:g.87588103T>A GRCh37
NC_000008.9:g.87657219T>A NCBI36
NG_016980.1:g.172801A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2359A>T MANE Select ENSP00000316605.5:p.Ser787Cys
ENST00000681546.1:n.2179A>T
ENST00000681746.1:c.*770A>T ENSP00000505959.1:n.*770A>T
ENST00000320005.5:c.2359A>T ENSP00000316605.5:p.Ser787Cys
ENST00000517327.5:c.276+2814A>T ENSP00000428329.1:n.276+2814A>T
NM_019098.4:c.2359A>T NP_061971.3:p.Ser787Cys
XM_011517138.1:c.1945A>T XP_011515440.1:p.Ser649Cys
XM_011517138.2:c.1945A>T XP_011515440.1:p.Ser649Cys
NM_019098.5:c.2359A>T MANE Select NP_061971.3:p.Ser787Cys