Canonical Allele Identifier: CA1799826309
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668115G= , CM000670.2:g.86668115G= GRCh38
NC_000008.10:g.87680343G= , CM000670.1:g.87680343G= GRCh37
NC_000008.9:g.87749459G= NCBI36
NG_016980.1:g.80561C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.547C= MANE Select ENSP00000316605.5:p.His183=
ENST00000681746.1:c.547C= ENSP00000505959.1:p.His183=
ENST00000320005.5:c.547C= ENSP00000316605.5:p.His183=
NM_019098.4:c.547C= NP_061971.3:p.His183=
XM_011517138.1:c.133C= XP_011515440.1:p.His45=
XM_011517138.2:c.133C= XP_011515440.1:p.His45=
NM_019098.5:c.547C= MANE Select NP_061971.3:p.His183=