Canonical Allele Identifier: CA422808344
Gene: CRB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.197390326C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421196C>T , CM000663.2:g.197421196C>T GRCh38
NC_000001.10:g.197390326C>T , CM000663.1:g.197390326C>T GRCh37
NC_000001.9:g.195656949C>T NCBI36
NG_008483.1:g.157919C>T
NG_008483.2:g.224735C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1368C>T MANE Select ENSP00000356370.3:p.Cys456=
ENST00000638467.1:c.1368C>T ENSP00000491102.1:p.Cys456=
ENST00000681519.1:c.249C>T ENSP00000505267.1:p.Cys83=
ENST00000367397.1:c.-490C>T ENSP00000356367.1:n.-490C>T
ENST00000367399.6:c.1032C>T ENSP00000356369.2:p.Cys344=
ENST00000367400.7:c.1368C>T ENSP00000356370.3:p.Cys456=
ENST00000476483.1:n.328C>T
ENST00000484075.5:c.1368C>T ENSP00000433932.1:p.Cys456=
ENST00000535699.5:c.1161C>T ENSP00000438786.1:p.Cys387=
ENST00000538660.5:c.1368C>T ENSP00000438091.1:p.Cys456=
NM_001193640.1:c.1032C>T NP_001180569.1:p.Cys344=
NM_001257965.1:c.1161C>T NP_001244894.1:p.Cys387=
NM_001257966.1:c.1368C>T NP_001244895.1:p.Cys456=
NM_201253.2:c.1368C>T NP_957705.1:p.Cys456=
NR_047563.1:n.1577C>T
NR_047564.1:n.1577C>T
XM_011509365.1:c.1368C>T XP_011507667.1:p.Cys456=
XM_011509366.1:c.1368C>T XP_011507668.1:p.Cys456=
XM_011509367.1:c.1368C>T XP_011507669.1:p.Cys456=
XM_011509368.1:c.786C>T XP_011507670.1:p.Cys262=
XM_011509369.1:c.-190C>T XP_011507671.1:n.-190C>T
XM_011509365.2:c.1368C>T XP_011507667.1:p.Cys456=
XM_011509369.2:c.-190C>T XP_011507671.1:n.-190C>T
XM_017000851.1:c.525C>T XP_016856340.1:p.Cys175=
XM_017000852.1:c.1368C>T XP_016856341.1:p.Cys456=
NM_201253.3:c.1368C>T MANE Select NP_957705.1:p.Cys456=
NM_001193640.2:c.1032C>T NP_001180569.1:p.Cys344=
NM_001257965.2:c.1161C>T NP_001244894.1:p.Cys387=
NR_047563.2:n.1529C>T
NR_047564.2:n.1529C>T
NM_001257966.2:c.1368C>T NP_001244895.1:p.Cys456=