Canonical Allele Identifier: CA344044395

Gene: CRB1

Linked Data

• dbSNP Id: rs1263132284
• MyVariant Identifiers: chr1:g.197403992A>C (hg19) ; chr1:g.197434862A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434862A>C , CM000663.2:g.197434862A>C	GRCh38
NC_000001.10:g.197403992A>C , CM000663.1:g.197403992A>C	GRCh37
NC_000001.9:g.195670615A>C	NCBI36
NG_008483.1:g.171585A>C
NG_008483.2:g.238401A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2999A>C MANE Select	ENSP00000356370.3:p.Asn1000Thr
ENST00000638467.1:c.2999A>C	ENSP00000491102.1:p.Asn1000Thr
ENST00000681519.1:c.1880A>C	ENSP00000505267.1:p.Asn627Thr
ENST00000367397.1:c.1142A>C	ENSP00000356367.1:p.Asn381Thr
ENST00000367399.6:c.2663A>C	ENSP00000356369.2:p.Asn888Thr
ENST00000367400.7:c.2999A>C	ENSP00000356370.3:p.Asn1000Thr
ENST00000484075.5:c.2999A>C	ENSP00000433932.1:p.Asn1000Thr
ENST00000535699.5:c.2927A>C	ENSP00000438786.1:p.Asn976Thr
ENST00000538660.5:c.2129-738A>C	ENSP00000438091.1:n.2129-738A>C
NM_001193640.1:c.2663A>C	NP_001180569.1:p.Asn888Thr
NM_001257965.1:c.2927A>C	NP_001244894.1:p.Asn976Thr
NM_001257966.1:c.2129-738A>C	NP_001244895.1:n.2129-738A>C
NM_201253.2:c.2999A>C	NP_957705.1:p.Asn1000Thr
NR_047563.1:n.3000A>C
NR_047564.1:n.3208A>C
XM_011509365.1:c.2999A>C	XP_011507667.1:p.Asn1000Thr
XM_011509366.1:c.2999A>C	XP_011507668.1:p.Asn1000Thr
XM_011509367.1:c.2999A>C	XP_011507669.1:p.Asn1000Thr
XM_011509368.1:c.2417A>C	XP_011507670.1:p.Asn806Thr
XM_011509369.1:c.1442A>C	XP_011507671.1:p.Asn481Thr
XM_011509365.2:c.2999A>C	XP_011507667.1:p.Asn1000Thr
XM_011509369.2:c.1442A>C	XP_011507671.1:p.Asn481Thr
XM_017000851.1:c.2156A>C	XP_016856340.1:p.Asn719Thr
XM_017000852.1:c.3134A>C	XP_016856341.1:p.Asn1045Thr
NM_201253.3:c.2999A>C MANE Select	NP_957705.1:p.Asn1000Thr
NM_001193640.2:c.2663A>C	NP_001180569.1:p.Asn888Thr
NM_001257965.2:c.2927A>C	NP_001244894.1:p.Asn976Thr
NR_047563.2:n.2952A>C
NR_047564.2:n.3160A>C
NM_001257966.2:c.2129-738A>C	NP_001244895.1:n.2129-738A>C