Canonical Allele Identifier: CA371456687
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739677T>G , CM000670.2:g.86739677T>G GRCh38
NC_000008.10:g.87751905T>G , CM000670.1:g.87751905T>G GRCh37
NC_000008.9:g.87821021T>G NCBI36
NG_016980.1:g.8999A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.189A>C MANE Select ENSP00000316605.5:p.Glu63Asp
ENST00000681746.1:c.189A>C ENSP00000505959.1:p.Glu63Asp
ENST00000320005.5:c.189A>C ENSP00000316605.5:p.Glu63Asp
ENST00000519777.1:n.171A>C
NM_019098.4:c.189A>C NP_061971.3:p.Glu63Asp
NM_019098.5:c.189A>C MANE Select NP_061971.3:p.Glu63Asp