Canonical Allele Identifier: CA1877946875

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377090_123377091delinsTG , CM000671.2:g.123377090_123377091delinsTG	GRCh38
NC_000009.11:g.126139369_126139370delinsTG , CM000671.1:g.126139369_126139370delinsTG	GRCh37
NC_000009.10:g.125179190_125179191delinsTG	NCBI36
NG_051311.1:g.28026_28027delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*28_*29delinsTG MANE Select	ENSP00000362734.3:n.*28_*29delinsTG
ENST00000373631.7:c.*28_*29delinsTG	ENSP00000362734.3:n.*28_*29delinsTG
ENST00000460253.1:c.*28_*29delinsTG	ENSP00000435279.1:n.*28_*29delinsTG
NM_173689.6:c.*28_*29delinsTG	NP_775960.4:n.*28_*29delinsTG
NR_104603.1:n.3000_3001delinsTG
XM_005251934.1:c.*28_*29delinsTG	XP_005251991.1:n.*28_*29delinsTG
XM_011518556.1:c.*28_*29delinsTG	XP_011516858.1:n.*28_*29delinsTG
XM_011518557.1:c.*28_*29delinsTG	XP_011516859.1:n.*28_*29delinsTG
XM_011518558.1:c.*28_*29delinsTG	XP_011516860.1:n.*28_*29delinsTG
XM_005251934.3:c.*28_*29delinsTG	XP_005251991.1:n.*28_*29delinsTG
XM_011518556.3:c.*28_*29delinsTG	XP_011516858.1:n.*28_*29delinsTG
XM_011518557.3:c.*28_*29delinsTG	XP_011516859.1:n.*28_*29delinsTG
XM_011518558.3:c.*28_*29delinsTG	XP_011516860.1:n.*28_*29delinsTG
NM_173689.7:c.*28_*29delinsTG MANE Select	NP_775960.4:n.*28_*29delinsTG
NR_104603.2:n.3000_3001delinsTG