Canonical Allele Identifier: CA371444092
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87645011C>T (hg19) chr8:g.86632783C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86632783C>T , CM000670.2:g.86632783C>T GRCh38
NC_000008.10:g.87645011C>T , CM000670.1:g.87645011C>T GRCh37
NC_000008.9:g.87714127C>T NCBI36
NG_016980.1:g.115893G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1289G>A MANE Select ENSP00000316605.5:p.Gly430Glu
ENST00000681546.1:n.1109G>A
ENST00000681746.1:c.1289G>A ENSP00000505959.1:p.Gly430Glu
ENST00000320005.5:c.1289G>A ENSP00000316605.5:p.Gly430Glu
NM_019098.4:c.1289G>A NP_061971.3:p.Gly430Glu
XM_011517138.1:c.875G>A XP_011515440.1:p.Gly292Glu
XM_011517138.2:c.875G>A XP_011515440.1:p.Gly292Glu
NM_019098.5:c.1289G>A MANE Select NP_061971.3:p.Gly430Glu
Search 100 bp 5'
Search 100 bp 3'