Canonical Allele Identifier: CA180347925
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs965934678
MyVariant Identifiers: chr8:g.87655736T>C (hg19) chr8:g.86643508T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86643508T>C , CM000670.2:g.86643508T>C GRCh38
NC_000008.10:g.87655736T>C , CM000670.1:g.87655736T>C GRCh37
NC_000008.9:g.87724852T>C NCBI36
NG_016980.1:g.105168A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.1178+243A>G MANE Select ENSP00000316605.5:n.1178+243A>G
ENST00000681546.1:n.998+243A>G
ENST00000681746.1:c.1178+243A>G ENSP00000505959.1:n.1178+243A>G
ENST00000320005.5:c.1178+243A>G ENSP00000316605.5:n.1178+243A>G
NM_019098.4:c.1178+243A>G NP_061971.3:n.1178+243A>G
XM_011517138.1:c.764+243A>G XP_011515440.1:n.764+243A>G
XM_011517138.2:c.764+243A>G XP_011515440.1:n.764+243A>G
NM_019098.5:c.1178+243A>G MANE Select NP_061971.3:n.1178+243A>G
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