Canonical Allele Identifier: CA1799781566
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86574089G= , CM000670.2:g.86574089G= GRCh38
NC_000008.10:g.87586317G= , CM000670.1:g.87586317G= GRCh37
NC_000008.9:g.87655433G= NCBI36
NG_016980.1:g.174587C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681746.1:c.*2556C= ENSP00000505959.1:n.*2556C=
ENST00000320005.5:c.*1715C= ENSP00000316605.5:n.*1715C=
ENST00000517327.5:c.276+4600C= ENSP00000428329.1:n.276+4600C=
NM_019098.4:c.*1715C= NP_061971.3:n.*1715C=
XM_011517138.1:c.*1715C= XP_011515440.1:n.*1715C=
XM_011517138.2:c.*1715C= XP_011515440.1:n.*1715C=