Canonical Allele Identifier: CA856343560
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1190317348
gnomAD v3: 8-86671509-T-G
gnomAD v4: 8-86671509-T-G
MyVariant Identifiers: chr8:g.87683737T>G (hg19) chr8:g.86671509T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671509T>G , CM000670.2:g.86671509T>G GRCh38
NC_000008.10:g.87683737T>G , CM000670.1:g.87683737T>G GRCh37
NC_000008.9:g.87752853T>G NCBI36
NG_016980.1:g.77167A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-411A>C MANE Select ENSP00000316605.5:n.339-411A>C
ENST00000680314.1:n.100-411A>C
ENST00000681746.1:c.339-411A>C ENSP00000505959.1:n.339-411A>C
ENST00000320005.5:c.339-411A>C ENSP00000316605.5:n.339-411A>C
NM_019098.4:c.339-411A>C NP_061971.3:n.339-411A>C
XM_011517138.1:c.-76-411A>C XP_011515440.1:n.-76-411A>C
XM_011517138.2:c.-76-411A>C XP_011515440.1:n.-76-411A>C
NM_019098.5:c.339-411A>C MANE Select NP_061971.3:n.339-411A>C
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