Canonical Allele Identifier: CA1799829740
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86670989A= , CM000670.2:g.86670989A= GRCh38
NC_000008.10:g.87683217A= , CM000670.1:g.87683217A= GRCh37
NC_000008.9:g.87752333A= NCBI36
NG_016980.1:g.77687T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.448T= MANE Select ENSP00000316605.5:p.Leu150=
ENST00000680314.1:n.209T=
ENST00000681746.1:c.448T= ENSP00000505959.1:p.Leu150=
ENST00000320005.5:c.448T= ENSP00000316605.5:p.Leu150=
NM_019098.4:c.448T= NP_061971.3:p.Leu150=
XM_011517138.1:c.34T= XP_011515440.1:p.Leu12=
XM_011517138.2:c.34T= XP_011515440.1:p.Leu12=
NM_019098.5:c.448T= MANE Select NP_061971.3:p.Leu150=