Canonical Allele Identifier: CA2649673045
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197478033A>G , CM000663.2:g.197478033A>G GRCh38
NC_000001.10:g.197447163A>G , CM000663.1:g.197447163A>G GRCh37
NC_000001.9:g.195713786A>G NCBI36
NG_008483.1:g.214756A>G
NG_008483.2:g.281572A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.*154A>G MANE Select ENSP00000356370.3:n.*154A>G
ENST00000367400.7:c.*154A>G ENSP00000356370.3:n.*154A>G
ENST00000448952.1:c.609A>G ENSP00000395407.1:n.609A>G
ENST00000484075.5:c.*486A>G ENSP00000433932.1:n.*486A>G
ENST00000535699.5:c.*154A>G ENSP00000438786.1:n.*154A>G
ENST00000538660.5:c.*154A>G ENSP00000438091.1:n.*154A>G
NM_001193640.1:c.*154A>G NP_001180569.1:n.*154A>G
NM_001257965.1:c.*154A>G NP_001244894.1:n.*154A>G
NM_001257966.1:c.*154A>G NP_001244895.1:n.*154A>G
NM_201253.2:c.*154A>G NP_957705.1:n.*154A>G
NR_047563.1:n.4376A>G
NR_047564.1:n.4826A>G
XM_011509366.1:c.*480A>G XP_011507668.1:n.*480A>G
XM_011509367.1:c.*354A>G XP_011507669.1:n.*354A>G
XM_011509368.1:c.*154A>G XP_011507670.1:n.*154A>G
XM_011509369.1:c.*154A>G XP_011507671.1:n.*154A>G
XM_011509369.2:c.*154A>G XP_011507671.1:n.*154A>G
XM_017000851.1:c.*154A>G XP_016856340.1:n.*154A>G
XM_017000852.1:c.*154A>G XP_016856341.1:n.*154A>G
NM_201253.3:c.*154A>G MANE Select NP_957705.1:n.*154A>G
NM_001193640.2:c.*154A>G NP_001180569.1:n.*154A>G
NM_001257965.2:c.*154A>G NP_001244894.1:n.*154A>G
NR_047563.2:n.4328A>G
NR_047564.2:n.4778A>G
NM_001257966.2:c.*154A>G NP_001244895.1:n.*154A>G