Canonical Allele Identifier: CA2781150517

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86643660del , CM000670.2:g.86643660del	GRCh38
NC_000008.10:g.87655888del , CM000670.1:g.87655888del	GRCh37
NC_000008.9:g.87725004del	NCBI36
NG_016980.1:g.105016del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1178+91del MANE Select	ENSP00000316605.5:n.1178+91del
ENST00000681546.1:n.998+91del
ENST00000681746.1:c.1178+91del	ENSP00000505959.1:n.1178+91del
ENST00000320005.5:c.1178+91del	ENSP00000316605.5:n.1178+91del
NM_019098.4:c.1178+91del	NP_061971.3:n.1178+91del
XM_011517138.1:c.764+91del	XP_011515440.1:n.764+91del
XM_011517138.2:c.764+91del	XP_011515440.1:n.764+91del
NM_019098.5:c.1178+91del MANE Select	NP_061971.3:n.1178+91del