Canonical Allele Identifier: CA371447963
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579206C>A , CM000670.2:g.86579206C>A GRCh38
NC_000008.10:g.87591434C>A , CM000670.1:g.87591434C>A GRCh37
NC_000008.9:g.87660550C>A NCBI36
NG_016980.1:g.169470G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1828G>T MANE Select ENSP00000316605.5:p.Ala610Ser
ENST00000681546.1:n.1648G>T
ENST00000681746.1:c.*239G>T ENSP00000505959.1:n.*239G>T
ENST00000320005.5:c.1828G>T ENSP00000316605.5:p.Ala610Ser
ENST00000517327.5:c.1G>T ENSP00000428329.1:p.Ala1Ser
NM_019098.4:c.1828G>T NP_061971.3:p.Ala610Ser
XM_011517138.1:c.1414G>T XP_011515440.1:p.Ala472Ser
XM_011517138.2:c.1414G>T XP_011515440.1:p.Ala472Ser
NM_019098.5:c.1828G>T MANE Select NP_061971.3:p.Ala610Ser