Canonical Allele Identifier: CA1799826291
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668102_86668106delinsAGCCT , CM000670.2:g.86668102_86668106delinsAGCCT GRCh38
NC_000008.10:g.87680330_87680334delinsAGCCT , CM000670.1:g.87680330_87680334delinsAGCCT GRCh37
NC_000008.9:g.87749446_87749450delinsAGCCT NCBI36
NG_016980.1:g.80570_80574delinsAGGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.556_560delinsAGGCT MANE Select ENSP00000316605.5:p.Arg186=
ENST00000681746.1:c.556_560delinsAGGCT ENSP00000505959.1:p.Arg186=
ENST00000320005.5:c.556_560delinsAGGCT ENSP00000316605.5:p.Arg186=
NM_019098.4:c.556_560delinsAGGCT NP_061971.3:p.Arg186=
XM_011517138.1:c.142_146delinsAGGCT XP_011515440.1:p.Arg48=
XM_011517138.2:c.142_146delinsAGGCT XP_011515440.1:p.Arg48=
NM_019098.5:c.556_560delinsAGGCT MANE Select NP_061971.3:p.Arg186=