Canonical Allele Identifier: CA371449898
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668113A>T , CM000670.2:g.86668113A>T GRCh38
NC_000008.10:g.87680341A>T , CM000670.1:g.87680341A>T GRCh37
NC_000008.9:g.87749457A>T NCBI36
NG_016980.1:g.80563T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.549T>A MANE Select ENSP00000316605.5:p.His183Gln
ENST00000681746.1:c.549T>A ENSP00000505959.1:p.His183Gln
ENST00000320005.5:c.549T>A ENSP00000316605.5:p.His183Gln
NM_019098.4:c.549T>A NP_061971.3:p.His183Gln
XM_011517138.1:c.135T>A XP_011515440.1:p.His45Gln
XM_011517138.2:c.135T>A XP_011515440.1:p.His45Gln
NM_019098.5:c.549T>A MANE Select NP_061971.3:p.His183Gln