Canonical Allele Identifier: CA1218087333
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1571646200

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197477974A>C , CM000663.2:g.197477974A>C GRCh38
NC_000001.10:g.197447104A>C , CM000663.1:g.197447104A>C GRCh37
NC_000001.9:g.195713727A>C NCBI36
NG_008483.1:g.214697A>C
NG_008483.2:g.281513A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.*95A>C MANE Select ENSP00000356370.3:n.*95A>C
ENST00000367400.7:c.*95A>C ENSP00000356370.3:n.*95A>C
ENST00000448952.1:c.550A>C ENSP00000395407.1:n.550A>C
ENST00000484075.5:c.*427A>C ENSP00000433932.1:n.*427A>C
ENST00000535699.5:c.*95A>C ENSP00000438786.1:n.*95A>C
ENST00000538660.5:c.*95A>C ENSP00000438091.1:n.*95A>C
NM_001193640.1:c.*95A>C NP_001180569.1:n.*95A>C
NM_001257965.1:c.*95A>C NP_001244894.1:n.*95A>C
NM_001257966.1:c.*95A>C NP_001244895.1:n.*95A>C
NM_201253.2:c.*95A>C NP_957705.1:n.*95A>C
NR_047563.1:n.4317A>C
NR_047564.1:n.4767A>C
XM_011509366.1:c.*421A>C XP_011507668.1:n.*421A>C
XM_011509367.1:c.*295A>C XP_011507669.1:n.*295A>C
XM_011509368.1:c.*95A>C XP_011507670.1:n.*95A>C
XM_011509369.1:c.*95A>C XP_011507671.1:n.*95A>C
XM_011509369.2:c.*95A>C XP_011507671.1:n.*95A>C
XM_017000851.1:c.*95A>C XP_016856340.1:n.*95A>C
XM_017000852.1:c.*95A>C XP_016856341.1:n.*95A>C
NM_201253.3:c.*95A>C MANE Select NP_957705.1:n.*95A>C
NM_001193640.2:c.*95A>C NP_001180569.1:n.*95A>C
NM_001257965.2:c.*95A>C NP_001244894.1:n.*95A>C
NR_047563.2:n.4269A>C
NR_047564.2:n.4719A>C
NM_001257966.2:c.*95A>C NP_001244895.1:n.*95A>C