Canonical Allele Identifier: CA1799784090
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575882G= , CM000670.2:g.86575882G= GRCh38
NC_000008.10:g.87588110G= , CM000670.1:g.87588110G= GRCh37
NC_000008.9:g.87657226G= NCBI36
NG_016980.1:g.172794C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2352C= MANE Select ENSP00000316605.5:p.Leu784=
ENST00000681546.1:n.2172C=
ENST00000681746.1:c.*763C= ENSP00000505959.1:n.*763C=
ENST00000320005.5:c.2352C= ENSP00000316605.5:p.Leu784=
ENST00000517327.5:c.276+2807C= ENSP00000428329.1:n.276+2807C=
NM_019098.4:c.2352C= NP_061971.3:p.Leu784=
XM_011517138.1:c.1938C= XP_011515440.1:p.Leu646=
XM_011517138.2:c.1938C= XP_011515440.1:p.Leu646=
NM_019098.5:c.2352C= MANE Select NP_061971.3:p.Leu784=