Canonical Allele Identifier: CA1799830244
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647887A= , CM000670.2:g.86647887A= GRCh38
NC_000008.10:g.87660115A= , CM000670.1:g.87660115A= GRCh37
NC_000008.9:g.87729231A= NCBI36
NG_016980.1:g.100789T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.904T= MANE Select ENSP00000316605.5:p.Leu302=
ENST00000681546.1:n.724T=
ENST00000681746.1:c.904T= ENSP00000505959.1:p.Leu302=
ENST00000320005.5:c.904T= ENSP00000316605.5:p.Leu302=
NM_019098.4:c.904T= NP_061971.3:p.Leu302=
XM_011517138.1:c.490T= XP_011515440.1:p.Leu164=
XM_011517138.2:c.490T= XP_011515440.1:p.Leu164=
NM_019098.5:c.904T= MANE Select NP_061971.3:p.Leu302=