Canonical Allele Identifier: CA371446316
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575978G>T , CM000670.2:g.86575978G>T GRCh38
NC_000008.10:g.87588206G>T , CM000670.1:g.87588206G>T GRCh37
NC_000008.9:g.87657322G>T NCBI36
NG_016980.1:g.172698C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2256C>A MANE Select ENSP00000316605.5:p.Asp752Glu
ENST00000681546.1:n.2076C>A
ENST00000681746.1:c.*667C>A ENSP00000505959.1:n.*667C>A
ENST00000320005.5:c.2256C>A ENSP00000316605.5:p.Asp752Glu
ENST00000517327.5:c.276+2711C>A ENSP00000428329.1:n.276+2711C>A
NM_019098.4:c.2256C>A NP_061971.3:p.Asp752Glu
XM_011517138.1:c.1842C>A XP_011515440.1:p.Asp614Glu
XM_011517138.2:c.1842C>A XP_011515440.1:p.Asp614Glu
NM_019098.5:c.2256C>A MANE Select NP_061971.3:p.Asp752Glu