Canonical Allele Identifier: CA856375091
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1243638355
MyVariant Identifiers: chr8:g.87587767A>C (hg19) chr8:g.86575539A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575539A>C , CM000670.2:g.86575539A>C GRCh38
NC_000008.10:g.87587767A>C , CM000670.1:g.87587767A>C GRCh37
NC_000008.9:g.87656883A>C NCBI36
NG_016980.1:g.173137T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.*265T>G MANE Select ENSP00000316605.5:n.*265T>G
ENST00000681546.1:n.2515T>G
ENST00000681746.1:c.*1106T>G ENSP00000505959.1:n.*1106T>G
ENST00000320005.5:c.*265T>G ENSP00000316605.5:n.*265T>G
ENST00000517327.5:c.276+3150T>G ENSP00000428329.1:n.276+3150T>G
NM_019098.4:c.*265T>G NP_061971.3:n.*265T>G
XM_011517138.1:c.*265T>G XP_011515440.1:n.*265T>G
XM_011517138.2:c.*265T>G XP_011515440.1:n.*265T>G
NM_019098.5:c.*265T>G MANE Select NP_061971.3:n.*265T>G
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