Canonical Allele Identifier: CA1799781541
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86574066A= , CM000670.2:g.86574066A= GRCh38
NC_000008.10:g.87586294A= , CM000670.1:g.87586294A= GRCh37
NC_000008.9:g.87655410A= NCBI36
NG_016980.1:g.174610T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681746.1:c.*2579T= ENSP00000505959.1:n.*2579T=
ENST00000320005.5:c.*1738T= ENSP00000316605.5:n.*1738T=
ENST00000517327.5:c.276+4623T= ENSP00000428329.1:n.276+4623T=
NM_019098.4:c.*1738T= NP_061971.3:n.*1738T=
XM_011517138.1:c.*1738T= XP_011515440.1:n.*1738T=
XM_011517138.2:c.*1738T= XP_011515440.1:n.*1738T=