Canonical Allele Identifier: CA422672532

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403897T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434767T>C , CM000663.2:g.197434767T>C	GRCh38
NC_000001.10:g.197403897T>C , CM000663.1:g.197403897T>C	GRCh37
NC_000001.9:g.195670520T>C	NCBI36
NG_008483.1:g.171490T>C
NG_008483.2:g.238306T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2904T>C MANE Select	ENSP00000356370.3:p.Asn968=
ENST00000638467.1:c.2904T>C	ENSP00000491102.1:p.Asn968=
ENST00000681519.1:c.1785T>C	ENSP00000505267.1:p.Asn595=
ENST00000367397.1:c.1047T>C	ENSP00000356367.1:p.Asn349=
ENST00000367399.6:c.2568T>C	ENSP00000356369.2:p.Asn856=
ENST00000367400.7:c.2904T>C	ENSP00000356370.3:p.Asn968=
ENST00000484075.5:c.2904T>C	ENSP00000433932.1:p.Asn968=
ENST00000535699.5:c.2832T>C	ENSP00000438786.1:p.Asn944=
ENST00000538660.5:c.2129-833T>C	ENSP00000438091.1:n.2129-833T>C
NM_001193640.1:c.2568T>C	NP_001180569.1:p.Asn856=
NM_001257965.1:c.2832T>C	NP_001244894.1:p.Asn944=
NM_001257966.1:c.2129-833T>C	NP_001244895.1:n.2129-833T>C
NM_201253.2:c.2904T>C	NP_957705.1:p.Asn968=
NR_047563.1:n.2905T>C
NR_047564.1:n.3113T>C
XM_011509365.1:c.2904T>C	XP_011507667.1:p.Asn968=
XM_011509366.1:c.2904T>C	XP_011507668.1:p.Asn968=
XM_011509367.1:c.2904T>C	XP_011507669.1:p.Asn968=
XM_011509368.1:c.2322T>C	XP_011507670.1:p.Asn774=
XM_011509369.1:c.1347T>C	XP_011507671.1:p.Asn449=
XM_011509365.2:c.2904T>C	XP_011507667.1:p.Asn968=
XM_011509369.2:c.1347T>C	XP_011507671.1:p.Asn449=
XM_017000851.1:c.2061T>C	XP_016856340.1:p.Asn687=
XM_017000852.1:c.3039T>C	XP_016856341.1:p.Asn1013=
NM_201253.3:c.2904T>C MANE Select	NP_957705.1:p.Asn968=
NM_001193640.2:c.2568T>C	NP_001180569.1:p.Asn856=
NM_001257965.2:c.2832T>C	NP_001244894.1:p.Asn944=
NR_047563.2:n.2857T>C
NR_047564.2:n.3065T>C
NM_001257966.2:c.2129-833T>C	NP_001244895.1:n.2129-833T>C