Canonical Allele Identifier: CA1799889858
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739546A= , CM000670.2:g.86739546A= GRCh38
NC_000008.10:g.87751774A= , CM000670.1:g.87751774A= GRCh37
NC_000008.9:g.87820890A= NCBI36
NG_016980.1:g.9130T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.211+109T= MANE Select ENSP00000316605.5:n.211+109T=
ENST00000681746.1:c.211+109T= ENSP00000505959.1:n.211+109T=
ENST00000320005.5:c.211+109T= ENSP00000316605.5:n.211+109T=
ENST00000519777.1:n.193+109T=
NM_019098.4:c.211+109T= NP_061971.3:n.211+109T=
NM_019098.5:c.211+109T= MANE Select NP_061971.3:n.211+109T=