Canonical Allele Identifier: CA1799826175
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668025A= , CM000670.2:g.86668025A= GRCh38
NC_000008.10:g.87680253A= , CM000670.1:g.87680253A= GRCh37
NC_000008.9:g.87749369A= NCBI36
NG_016980.1:g.80651T=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.637T= MANE Select ENSP00000316605.5:p.Tyr213=
ENST00000681746.1:c.637T= ENSP00000505959.1:p.Tyr213=
ENST00000320005.5:c.637T= ENSP00000316605.5:p.Tyr213=
NM_019098.4:c.637T= NP_061971.3:p.Tyr213=
XM_011517138.1:c.223T= XP_011515440.1:p.Tyr75=
XM_011517138.2:c.223T= XP_011515440.1:p.Tyr75=
NM_019098.5:c.637T= MANE Select NP_061971.3:p.Tyr213=