Canonical Allele Identifier: CA371447700
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579113T>A , CM000670.2:g.86579113T>A GRCh38
NC_000008.10:g.87591341T>A , CM000670.1:g.87591341T>A GRCh37
NC_000008.9:g.87660457T>A NCBI36
NG_016980.1:g.169563A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1921A>T MANE Select ENSP00000316605.5:p.Lys641Ter
ENST00000681546.1:n.1741A>T
ENST00000681746.1:c.*332A>T ENSP00000505959.1:n.*332A>T
ENST00000320005.5:c.1921A>T ENSP00000316605.5:p.Lys641Ter
ENST00000517327.5:c.94A>T ENSP00000428329.1:p.Lys32Ter
NM_019098.4:c.1921A>T NP_061971.3:p.Lys641Ter
XM_011517138.1:c.1507A>T XP_011515440.1:p.Lys503Ter
XM_011517138.2:c.1507A>T XP_011515440.1:p.Lys503Ter
NM_019098.5:c.1921A>T MANE Select NP_061971.3:p.Lys641Ter