Canonical Allele Identifier: CA344032905
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1558126931

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421749G>A , CM000663.2:g.197421749G>A GRCh38
NC_000001.10:g.197390879G>A , CM000663.1:g.197390879G>A GRCh37
NC_000001.9:g.195657502G>A NCBI36
NG_008483.1:g.158472G>A
NG_008483.2:g.225288G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1921G>A MANE Select ENSP00000356370.3:p.Gly641Ser
ENST00000638467.1:c.1921G>A ENSP00000491102.1:p.Gly641Ser
ENST00000681519.1:c.802G>A ENSP00000505267.1:p.Gly268Ser
ENST00000367397.1:c.64G>A ENSP00000356367.1:p.Gly22Ser
ENST00000367399.6:c.1585G>A ENSP00000356369.2:p.Gly529Ser
ENST00000367400.7:c.1921G>A ENSP00000356370.3:p.Gly641Ser
ENST00000484075.5:c.1921G>A ENSP00000433932.1:p.Gly641Ser
ENST00000535699.5:c.1714G>A ENSP00000438786.1:p.Gly572Ser
ENST00000538660.5:c.1921G>A ENSP00000438091.1:p.Gly641Ser
NM_001193640.1:c.1585G>A NP_001180569.1:p.Gly529Ser
NM_001257965.1:c.1714G>A NP_001244894.1:p.Gly572Ser
NM_001257966.1:c.1921G>A NP_001244895.1:p.Gly641Ser
NM_201253.2:c.1921G>A NP_957705.1:p.Gly641Ser
NR_047563.1:n.1923-1G>A
NR_047564.1:n.2130G>A
XM_011509365.1:c.1921G>A XP_011507667.1:p.Gly641Ser
XM_011509366.1:c.1921G>A XP_011507668.1:p.Gly641Ser
XM_011509367.1:c.1921G>A XP_011507669.1:p.Gly641Ser
XM_011509368.1:c.1339G>A XP_011507670.1:p.Gly447Ser
XM_011509369.1:c.364G>A XP_011507671.1:p.Gly122Ser
XM_011509365.2:c.1921G>A XP_011507667.1:p.Gly641Ser
XM_011509369.2:c.364G>A XP_011507671.1:p.Gly122Ser
XM_017000851.1:c.1078G>A XP_016856340.1:p.Gly360Ser
XM_017000852.1:c.1921G>A XP_016856341.1:p.Gly641Ser
NM_201253.3:c.1921G>A MANE Select NP_957705.1:p.Gly641Ser
NM_001193640.2:c.1585G>A NP_001180569.1:p.Gly529Ser
NM_001257965.2:c.1714G>A NP_001244894.1:p.Gly572Ser
NR_047563.2:n.1875-1G>A
NR_047564.2:n.2082G>A
NM_001257966.2:c.1921G>A NP_001244895.1:p.Gly641Ser