Canonical Allele Identifier: CA461831083
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87680251G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668023G>A , CM000670.2:g.86668023G>A GRCh38
NC_000008.10:g.87680251G>A , CM000670.1:g.87680251G>A GRCh37
NC_000008.9:g.87749367G>A NCBI36
NG_016980.1:g.80653C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.639C>T MANE Select ENSP00000316605.5:p.Tyr213=
ENST00000681746.1:c.639C>T ENSP00000505959.1:p.Tyr213=
ENST00000320005.5:c.639C>T ENSP00000316605.5:p.Tyr213=
NM_019098.4:c.639C>T NP_061971.3:p.Tyr213=
XM_011517138.1:c.225C>T XP_011515440.1:p.Tyr75=
XM_011517138.2:c.225C>T XP_011515440.1:p.Tyr75=
NM_019098.5:c.639C>T MANE Select NP_061971.3:p.Tyr213=