Canonical Allele Identifier: CA1799890185
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739713T= , CM000670.2:g.86739713T= GRCh38
NC_000008.10:g.87751941T= , CM000670.1:g.87751941T= GRCh37
NC_000008.9:g.87821057T= NCBI36
NG_016980.1:g.8963A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.153A= MANE Select ENSP00000316605.5:p.Lys51=
ENST00000681746.1:c.153A= ENSP00000505959.1:p.Lys51=
ENST00000320005.5:c.153A= ENSP00000316605.5:p.Lys51=
ENST00000519777.1:n.135A=
NM_019098.4:c.153A= NP_061971.3:p.Lys51=
NM_019098.5:c.153A= MANE Select NP_061971.3:p.Lys51=