Canonical Allele Identifier: CA344044670

Gene: CRB1

Linked Data

• dbSNP Id: rs1665056137
• MyVariant Identifiers: chr1:g.197404018T>G (hg19) ; chr1:g.197434888T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434888T>G , CM000663.2:g.197434888T>G	GRCh38
NC_000001.10:g.197404018T>G , CM000663.1:g.197404018T>G	GRCh37
NC_000001.9:g.195670641T>G	NCBI36
NG_008483.1:g.171611T>G
NG_008483.2:g.238427T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3025T>G MANE Select	ENSP00000356370.3:p.Phe1009Val
ENST00000638467.1:c.3025T>G	ENSP00000491102.1:p.Phe1009Val
ENST00000681519.1:c.1906T>G	ENSP00000505267.1:p.Phe636Val
ENST00000367397.1:c.1168T>G	ENSP00000356367.1:p.Phe390Val
ENST00000367399.6:c.2689T>G	ENSP00000356369.2:p.Phe897Val
ENST00000367400.7:c.3025T>G	ENSP00000356370.3:p.Phe1009Val
ENST00000484075.5:c.3025T>G	ENSP00000433932.1:p.Phe1009Val
ENST00000535699.5:c.2953T>G	ENSP00000438786.1:p.Phe985Val
ENST00000538660.5:c.2129-712T>G	ENSP00000438091.1:n.2129-712T>G
NM_001193640.1:c.2689T>G	NP_001180569.1:p.Phe897Val
NM_001257965.1:c.2953T>G	NP_001244894.1:p.Phe985Val
NM_001257966.1:c.2129-712T>G	NP_001244895.1:n.2129-712T>G
NM_201253.2:c.3025T>G	NP_957705.1:p.Phe1009Val
NR_047563.1:n.3026T>G
NR_047564.1:n.3234T>G
XM_011509365.1:c.3025T>G	XP_011507667.1:p.Phe1009Val
XM_011509366.1:c.3025T>G	XP_011507668.1:p.Phe1009Val
XM_011509367.1:c.3025T>G	XP_011507669.1:p.Phe1009Val
XM_011509368.1:c.2443T>G	XP_011507670.1:p.Phe815Val
XM_011509369.1:c.1468T>G	XP_011507671.1:p.Phe490Val
XM_011509365.2:c.3025T>G	XP_011507667.1:p.Phe1009Val
XM_011509369.2:c.1468T>G	XP_011507671.1:p.Phe490Val
XM_017000851.1:c.2182T>G	XP_016856340.1:p.Phe728Val
XM_017000852.1:c.3160T>G	XP_016856341.1:p.Phe1054Val
NM_201253.3:c.3025T>G MANE Select	NP_957705.1:p.Phe1009Val
NM_001193640.2:c.2689T>G	NP_001180569.1:p.Phe897Val
NM_001257965.2:c.2953T>G	NP_001244894.1:p.Phe985Val
NR_047563.2:n.2978T>G
NR_047564.2:n.3186T>G
NM_001257966.2:c.2129-712T>G	NP_001244895.1:n.2129-712T>G