Canonical Allele Identifier: CA1799781725
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86574167G= , CM000670.2:g.86574167G= GRCh38
NC_000008.10:g.87586395G= , CM000670.1:g.87586395G= GRCh37
NC_000008.9:g.87655511G= NCBI36
NG_016980.1:g.174509C=

Transcript Alleles

HGVS Amino-acid change
ENST00000681746.1:c.*2478C= ENSP00000505959.1:n.*2478C=
ENST00000320005.5:c.*1637C= ENSP00000316605.5:n.*1637C=
ENST00000517327.5:c.276+4522C= ENSP00000428329.1:n.276+4522C=
NM_019098.4:c.*1637C= NP_061971.3:n.*1637C=
XM_011517138.1:c.*1637C= XP_011515440.1:n.*1637C=
XM_011517138.2:c.*1637C= XP_011515440.1:n.*1637C=