Canonical Allele Identifier: CA1799783469
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1821640594
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575494T>C , CM000670.2:g.86575494T>C GRCh38
NC_000008.10:g.87587722T>C , CM000670.1:g.87587722T>C GRCh37
NC_000008.9:g.87656838T>C NCBI36
NG_016980.1:g.173182A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.*310A>G MANE Select ENSP00000316605.5:n.*310A>G
ENST00000681546.1:n.2560A>G
ENST00000681746.1:c.*1151A>G ENSP00000505959.1:n.*1151A>G
ENST00000320005.5:c.*310A>G ENSP00000316605.5:n.*310A>G
ENST00000517327.5:c.276+3195A>G ENSP00000428329.1:n.276+3195A>G
NM_019098.4:c.*310A>G NP_061971.3:n.*310A>G
XM_011517138.1:c.*310A>G XP_011515440.1:n.*310A>G
XM_011517138.2:c.*310A>G XP_011515440.1:n.*310A>G
NM_019098.5:c.*310A>G MANE Select NP_061971.3:n.*310A>G
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