Canonical Allele Identifier: CA371450033
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87683176T>G (hg19) chr8:g.86670948T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86670948T>G , CM000670.2:g.86670948T>G GRCh38
NC_000008.10:g.87683176T>G , CM000670.1:g.87683176T>G GRCh37
NC_000008.9:g.87752292T>G NCBI36
NG_016980.1:g.77728A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.489A>C MANE Select ENSP00000316605.5:p.Gln163His
ENST00000680314.1:n.250A>C
ENST00000681746.1:c.489A>C ENSP00000505959.1:p.Gln163His
ENST00000320005.5:c.489A>C ENSP00000316605.5:p.Gln163His
NM_019098.4:c.489A>C NP_061971.3:p.Gln163His
XM_011517138.1:c.75A>C XP_011515440.1:p.Gln25His
XM_011517138.2:c.75A>C XP_011515440.1:p.Gln25His
NM_019098.5:c.489A>C MANE Select NP_061971.3:p.Gln163His
Search 100 bp 5'
Search 100 bp 3'