Canonical Allele Identifier: CA371449865
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668098C>A , CM000670.2:g.86668098C>A GRCh38
NC_000008.10:g.87680326C>A , CM000670.1:g.87680326C>A GRCh37
NC_000008.9:g.87749442C>A NCBI36
NG_016980.1:g.80578G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.564G>T MANE Select ENSP00000316605.5:p.Leu188Phe
ENST00000681746.1:c.564G>T ENSP00000505959.1:p.Leu188Phe
ENST00000320005.5:c.564G>T ENSP00000316605.5:p.Leu188Phe
NM_019098.4:c.564G>T NP_061971.3:p.Leu188Phe
XM_011517138.1:c.150G>T XP_011515440.1:p.Leu50Phe
XM_011517138.2:c.150G>T XP_011515440.1:p.Leu50Phe
NM_019098.5:c.564G>T MANE Select NP_061971.3:p.Leu188Phe