Canonical Allele Identifier: CA371449883
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668108T>A , CM000670.2:g.86668108T>A GRCh38
NC_000008.10:g.87680336T>A , CM000670.1:g.87680336T>A GRCh37
NC_000008.9:g.87749452T>A NCBI36
NG_016980.1:g.80568A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.554A>T MANE Select ENSP00000316605.5:p.Tyr185Phe
ENST00000681746.1:c.554A>T ENSP00000505959.1:p.Tyr185Phe
ENST00000320005.5:c.554A>T ENSP00000316605.5:p.Tyr185Phe
NM_019098.4:c.554A>T NP_061971.3:p.Tyr185Phe
XM_011517138.1:c.140A>T XP_011515440.1:p.Tyr47Phe
XM_011517138.2:c.140A>T XP_011515440.1:p.Tyr47Phe
NM_019098.5:c.554A>T MANE Select NP_061971.3:p.Tyr185Phe