Canonical Allele Identifier: CA371447966
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579208A>T , CM000670.2:g.86579208A>T GRCh38
NC_000008.10:g.87591436A>T , CM000670.1:g.87591436A>T GRCh37
NC_000008.9:g.87660552A>T NCBI36
NG_016980.1:g.169468T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1826T>A MANE Select ENSP00000316605.5:p.Val609Glu
ENST00000681546.1:n.1646T>A
ENST00000681746.1:c.*237T>A ENSP00000505959.1:n.*237T>A
ENST00000320005.5:c.1826T>A ENSP00000316605.5:p.Val609Glu
NM_019098.4:c.1826T>A NP_061971.3:p.Val609Glu
XM_011517138.1:c.1412T>A XP_011515440.1:p.Val471Glu
XM_011517138.2:c.1412T>A XP_011515440.1:p.Val471Glu
NM_019098.5:c.1826T>A MANE Select NP_061971.3:p.Val609Glu