Canonical Allele Identifier: CA461831176
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87683173A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86670945A>T , CM000670.2:g.86670945A>T GRCh38
NC_000008.10:g.87683173A>T , CM000670.1:g.87683173A>T GRCh37
NC_000008.9:g.87752289A>T NCBI36
NG_016980.1:g.77731T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.492T>A MANE Select ENSP00000316605.5:p.Thr164=
ENST00000680314.1:n.253T>A
ENST00000681746.1:c.492T>A ENSP00000505959.1:p.Thr164=
ENST00000320005.5:c.492T>A ENSP00000316605.5:p.Thr164=
NM_019098.4:c.492T>A NP_061971.3:p.Thr164=
XM_011517138.1:c.78T>A XP_011515440.1:p.Thr26=
XM_011517138.2:c.78T>A XP_011515440.1:p.Thr26=
NM_019098.5:c.492T>A MANE Select NP_061971.3:p.Thr164=
Search 100 bp 5'
Search 100 bp 3'