Canonical Allele Identifier: CA344045788

Gene: CRB1

Linked Data

• dbSNP Id: rs1457203962
• gnomAD v3: 1-197434986-G-T
• gnomAD v4: 1-197434986-G-T
• MyVariant Identifiers: chr1:g.197404116G>T (hg19) ; chr1:g.197434986G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434986G>T , CM000663.2:g.197434986G>T	GRCh38
NC_000001.10:g.197404116G>T , CM000663.1:g.197404116G>T	GRCh37
NC_000001.9:g.195670739G>T	NCBI36
NG_008483.1:g.171709G>T
NG_008483.2:g.238525G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3123G>T MANE Select	ENSP00000356370.3:p.Met1041Ile
ENST00000638467.1:c.3123G>T	ENSP00000491102.1:p.Met1041Ile
ENST00000681519.1:c.2004G>T	ENSP00000505267.1:p.Met668Ile
ENST00000367397.1:c.1266G>T	ENSP00000356367.1:p.Met422Ile
ENST00000367399.6:c.2787G>T	ENSP00000356369.2:p.Met929Ile
ENST00000367400.7:c.3123G>T	ENSP00000356370.3:p.Met1041Ile
ENST00000484075.5:c.3123G>T	ENSP00000433932.1:p.Met1041Ile
ENST00000535699.5:c.3051G>T	ENSP00000438786.1:p.Met1017Ile
ENST00000538660.5:c.2129-614G>T	ENSP00000438091.1:n.2129-614G>T
NM_001193640.1:c.2787G>T	NP_001180569.1:p.Met929Ile
NM_001257965.1:c.3051G>T	NP_001244894.1:p.Met1017Ile
NM_001257966.1:c.2129-614G>T	NP_001244895.1:n.2129-614G>T
NM_201253.2:c.3123G>T	NP_957705.1:p.Met1041Ile
NR_047563.1:n.3124G>T
NR_047564.1:n.3332G>T
XM_011509365.1:c.3123G>T	XP_011507667.1:p.Met1041Ile
XM_011509366.1:c.3123G>T	XP_011507668.1:p.Met1041Ile
XM_011509367.1:c.3123G>T	XP_011507669.1:p.Met1041Ile
XM_011509368.1:c.2541G>T	XP_011507670.1:p.Met847Ile
XM_011509369.1:c.1566G>T	XP_011507671.1:p.Met522Ile
XM_011509365.2:c.3123G>T	XP_011507667.1:p.Met1041Ile
XM_011509369.2:c.1566G>T	XP_011507671.1:p.Met522Ile
XM_017000851.1:c.2280G>T	XP_016856340.1:p.Met760Ile
XM_017000852.1:c.3258G>T	XP_016856341.1:p.Met1086Ile
NM_201253.3:c.3123G>T MANE Select	NP_957705.1:p.Met1041Ile
NM_001193640.2:c.2787G>T	NP_001180569.1:p.Met929Ile
NM_001257965.2:c.3051G>T	NP_001244894.1:p.Met1017Ile
NR_047563.2:n.3076G>T
NR_047564.2:n.3284G>T
NM_001257966.2:c.2129-614G>T	NP_001244895.1:n.2129-614G>T