Canonical Allele Identifier: CA2781158389

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86739638_86739639insTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000670.2:g.86739638_86739639insTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000008.10:g.87751866_87751867insTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000670.1:g.87751866_87751867insTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000008.9:g.87820982_87820983insTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_016980.1:g.9055_9056insAAAAAAAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	ENSP00000316605.5:n.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000681746.1:c.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000505959.1:n.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000320005.5:c.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000316605.5:n.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000519777.1:n.193+34_193+35insAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_019098.4:c.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_061971.3:n.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_019098.5:c.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	NP_061971.3:n.211+34_211+35insAAAAAAAAAAAAAAAAAAAAAAAAAA