Canonical Allele Identifier: CA1799889925
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739620_86739624delinsGTTTT , CM000670.2:g.86739620_86739624delinsGTTTT GRCh38
NC_000008.10:g.87751848_87751852delinsGTTTT , CM000670.1:g.87751848_87751852delinsGTTTT GRCh37
NC_000008.9:g.87820964_87820968delinsGTTTT NCBI36
NG_016980.1:g.9052_9056delinsAAAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.211+31_211+35delinsAAAAC MANE Select ENSP00000316605.5:n.211+31_211+35delinsAA...
ENST00000681746.1:c.211+31_211+35delinsAAAAC ENSP00000505959.1:n.211+31_211+35delinsAA...
ENST00000320005.5:c.211+31_211+35delinsAAAAC ENSP00000316605.5:n.211+31_211+35delinsAA...
ENST00000519777.1:n.193+31_193+35delinsAAAAC
NM_019098.4:c.211+31_211+35delinsAAAAC NP_061971.3:n.211+31_211+35delinsAAAAC
NM_019098.5:c.211+31_211+35delinsAAAAC MANE Select NP_061971.3:n.211+31_211+35delinsAAAAC