Canonical Allele Identifier: CA371447960
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579205G>T , CM000670.2:g.86579205G>T GRCh38
NC_000008.10:g.87591433G>T , CM000670.1:g.87591433G>T GRCh37
NC_000008.9:g.87660549G>T NCBI36
NG_016980.1:g.169471C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1829C>A MANE Select ENSP00000316605.5:p.Ala610Asp
ENST00000681546.1:n.1649C>A
ENST00000681746.1:c.*240C>A ENSP00000505959.1:n.*240C>A
ENST00000320005.5:c.1829C>A ENSP00000316605.5:p.Ala610Asp
ENST00000517327.5:c.2C>A ENSP00000428329.1:p.Ala1Asp
NM_019098.4:c.1829C>A NP_061971.3:p.Ala610Asp
XM_011517138.1:c.1415C>A XP_011515440.1:p.Ala472Asp
XM_011517138.2:c.1415C>A XP_011515440.1:p.Ala472Asp
NM_019098.5:c.1829C>A MANE Select NP_061971.3:p.Ala610Asp