Canonical Allele Identifier: CA1312316
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs115649214

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197435180A>T , CM000663.2:g.197435180A>T GRCh38
NC_000001.10:g.197404310A>T , CM000663.1:g.197404310A>T GRCh37
NC_000001.9:g.195670933A>T NCBI36
NG_008483.1:g.171903A>T
NG_008483.2:g.238719A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.3317A>T MANE Select ENSP00000356370.3:p.Tyr1106Phe
ENST00000638467.1:c.3317A>T ENSP00000491102.1:p.Tyr1106Phe
ENST00000681519.1:c.2198A>T ENSP00000505267.1:p.Tyr733Phe
ENST00000367397.1:c.1460A>T ENSP00000356367.1:p.Tyr487Phe
ENST00000367399.6:c.2981A>T ENSP00000356369.2:p.Tyr994Phe
ENST00000367400.7:c.3317A>T ENSP00000356370.3:p.Tyr1106Phe
ENST00000484075.5:c.3317A>T ENSP00000433932.1:p.Tyr1106Phe
ENST00000535699.5:c.3245A>T ENSP00000438786.1:p.Tyr1082Phe
ENST00000538660.5:c.2129-420A>T ENSP00000438091.1:n.2129-420A>T
NM_001193640.1:c.2981A>T NP_001180569.1:p.Tyr994Phe
NM_001257965.1:c.3245A>T NP_001244894.1:p.Tyr1082Phe
NM_001257966.1:c.2129-420A>T NP_001244895.1:n.2129-420A>T
NM_201253.2:c.3317A>T NP_957705.1:p.Tyr1106Phe
NR_047563.1:n.3318A>T
NR_047564.1:n.3526A>T
XM_011509365.1:c.3317A>T XP_011507667.1:p.Tyr1106Phe
XM_011509366.1:c.3317A>T XP_011507668.1:p.Tyr1106Phe
XM_011509367.1:c.3317A>T XP_011507669.1:p.Tyr1106Phe
XM_011509368.1:c.2735A>T XP_011507670.1:p.Tyr912Phe
XM_011509369.1:c.1760A>T XP_011507671.1:p.Tyr587Phe
XM_011509365.2:c.3317A>T XP_011507667.1:p.Tyr1106Phe
XM_011509369.2:c.1760A>T XP_011507671.1:p.Tyr587Phe
XM_017000851.1:c.2474A>T XP_016856340.1:p.Tyr825Phe
XM_017000852.1:c.3452A>T XP_016856341.1:p.Tyr1151Phe
NM_201253.3:c.3317A>T MANE Select NP_957705.1:p.Tyr1106Phe
NM_001193640.2:c.2981A>T NP_001180569.1:p.Tyr994Phe
NM_001257965.2:c.3245A>T NP_001244894.1:p.Tyr1082Phe
NR_047563.2:n.3270A>T
NR_047564.2:n.3478A>T
NM_001257966.2:c.2129-420A>T NP_001244895.1:n.2129-420A>T