Canonical Allele Identifier: CA422809177

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1671420
• ClinVar RCV Id: RCV002198903
• dbSNP Id: rs765210114
• gnomAD v4: 1-197427659-C-T
• MyVariant Identifiers: chr1:g.197396789C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427659C>T , CM000663.2:g.197427659C>T	GRCh38
NC_000001.10:g.197396789C>T , CM000663.1:g.197396789C>T	GRCh37
NC_000001.9:g.195663412C>T	NCBI36
NG_008483.1:g.164382C>T
NG_008483.2:g.231198C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2334C>T MANE Select	ENSP00000356370.3:p.Asn778=
ENST00000638467.1:c.2334C>T	ENSP00000491102.1:p.Asn778=
ENST00000681519.1:c.1215C>T	ENSP00000505267.1:p.Asn405=
ENST00000367397.1:c.477C>T	ENSP00000356367.1:p.Asn159=
ENST00000367399.6:c.1998C>T	ENSP00000356369.2:p.Asn666=
ENST00000367400.7:c.2334C>T	ENSP00000356370.3:p.Asn778=
ENST00000480086.2:n.235C>T
ENST00000484075.5:c.2334C>T	ENSP00000433932.1:p.Asn778=
ENST00000535699.5:c.2127C>T	ENSP00000438786.1:p.Asn709=
ENST00000538660.5:c.2128+5703C>T	ENSP00000438091.1:n.2128+5703C>T
NM_001193640.1:c.1998C>T	NP_001180569.1:p.Asn666=
NM_001257965.1:c.2127C>T	NP_001244894.1:p.Asn709=
NM_001257966.1:c.2128+5703C>T	NP_001244895.1:n.2128+5703C>T
NM_201253.2:c.2334C>T	NP_957705.1:p.Asn778=
NR_047563.1:n.2335C>T
NR_047564.1:n.2543C>T
XM_011509365.1:c.2334C>T	XP_011507667.1:p.Asn778=
XM_011509366.1:c.2334C>T	XP_011507668.1:p.Asn778=
XM_011509367.1:c.2334C>T	XP_011507669.1:p.Asn778=
XM_011509368.1:c.1752C>T	XP_011507670.1:p.Asn584=
XM_011509369.1:c.777C>T	XP_011507671.1:p.Asn259=
XM_011509365.2:c.2334C>T	XP_011507667.1:p.Asn778=
XM_011509369.2:c.777C>T	XP_011507671.1:p.Asn259=
XM_017000851.1:c.1491C>T	XP_016856340.1:p.Asn497=
XM_017000852.1:c.2334C>T	XP_016856341.1:p.Asn778=
NM_201253.3:c.2334C>T MANE Select	NP_957705.1:p.Asn778=
NM_001193640.2:c.1998C>T	NP_001180569.1:p.Asn666=
NM_001257965.2:c.2127C>T	NP_001244894.1:p.Asn709=
NR_047563.2:n.2287C>T
NR_047564.2:n.2495C>T
NM_001257966.2:c.2128+5703C>T	NP_001244895.1:n.2128+5703C>T