Canonical Allele Identifier: CA371446464
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86576042T>C , CM000670.2:g.86576042T>C GRCh38
NC_000008.10:g.87588270T>C , CM000670.1:g.87588270T>C GRCh37
NC_000008.9:g.87657386T>C NCBI36
NG_016980.1:g.172634A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.2192A>G MANE Select ENSP00000316605.5:p.Glu731Gly
ENST00000681546.1:n.2012A>G
ENST00000681746.1:c.*603A>G ENSP00000505959.1:n.*603A>G
ENST00000320005.5:c.2192A>G ENSP00000316605.5:p.Glu731Gly
ENST00000517327.5:c.276+2647A>G ENSP00000428329.1:n.276+2647A>G
NM_019098.4:c.2192A>G NP_061971.3:p.Glu731Gly
XM_011517138.1:c.1778A>G XP_011515440.1:p.Glu593Gly
XM_011517138.2:c.1778A>G XP_011515440.1:p.Glu593Gly
NM_019098.5:c.2192A>G MANE Select NP_061971.3:p.Glu731Gly