Canonical Allele Identifier: CA1799783624
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1585940707
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575609G>T , CM000670.2:g.86575609G>T GRCh38
NC_000008.10:g.87587837G>T , CM000670.1:g.87587837G>T GRCh37
NC_000008.9:g.87656953G>T NCBI36
NG_016980.1:g.173067C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.*195C>A MANE Select ENSP00000316605.5:n.*195C>A
ENST00000681546.1:n.2445C>A
ENST00000681746.1:c.*1036C>A ENSP00000505959.1:n.*1036C>A
ENST00000320005.5:c.*195C>A ENSP00000316605.5:n.*195C>A
ENST00000517327.5:c.276+3080C>A ENSP00000428329.1:n.276+3080C>A
NM_019098.4:c.*195C>A NP_061971.3:n.*195C>A
XM_011517138.1:c.*195C>A XP_011515440.1:n.*195C>A
XM_011517138.2:c.*195C>A XP_011515440.1:n.*195C>A
NM_019098.5:c.*195C>A MANE Select NP_061971.3:n.*195C>A
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