Canonical Allele Identifier: CA35906883

Gene: CRB1

Linked Data

• dbSNP Id: rs1052646716
• gnomAD v3: 1-197434908-C-T
• gnomAD v4: 1-197434908-C-T
• MyVariant Identifiers: chr1:g.197404038C>T (hg19) ; chr1:g.197434908C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434908C>T , CM000663.2:g.197434908C>T	GRCh38
NC_000001.10:g.197404038C>T , CM000663.1:g.197404038C>T	GRCh37
NC_000001.9:g.195670661C>T	NCBI36
NG_008483.1:g.171631C>T
NG_008483.2:g.238447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3045C>T MANE Select	ENSP00000356370.3:p.Gly1015=
ENST00000638467.1:c.3045C>T	ENSP00000491102.1:p.Gly1015=
ENST00000681519.1:c.1926C>T	ENSP00000505267.1:p.Gly642=
ENST00000367397.1:c.1188C>T	ENSP00000356367.1:p.Gly396=
ENST00000367399.6:c.2709C>T	ENSP00000356369.2:p.Gly903=
ENST00000367400.7:c.3045C>T	ENSP00000356370.3:p.Gly1015=
ENST00000484075.5:c.3045C>T	ENSP00000433932.1:p.Gly1015=
ENST00000535699.5:c.2973C>T	ENSP00000438786.1:p.Gly991=
ENST00000538660.5:c.2129-692C>T	ENSP00000438091.1:n.2129-692C>T
NM_001193640.1:c.2709C>T	NP_001180569.1:p.Gly903=
NM_001257965.1:c.2973C>T	NP_001244894.1:p.Gly991=
NM_001257966.1:c.2129-692C>T	NP_001244895.1:n.2129-692C>T
NM_201253.2:c.3045C>T	NP_957705.1:p.Gly1015=
NR_047563.1:n.3046C>T
NR_047564.1:n.3254C>T
XM_011509365.1:c.3045C>T	XP_011507667.1:p.Gly1015=
XM_011509366.1:c.3045C>T	XP_011507668.1:p.Gly1015=
XM_011509367.1:c.3045C>T	XP_011507669.1:p.Gly1015=
XM_011509368.1:c.2463C>T	XP_011507670.1:p.Gly821=
XM_011509369.1:c.1488C>T	XP_011507671.1:p.Gly496=
XM_011509365.2:c.3045C>T	XP_011507667.1:p.Gly1015=
XM_011509369.2:c.1488C>T	XP_011507671.1:p.Gly496=
XM_017000851.1:c.2202C>T	XP_016856340.1:p.Gly734=
XM_017000852.1:c.3180C>T	XP_016856341.1:p.Gly1060=
NM_201253.3:c.3045C>T MANE Select	NP_957705.1:p.Gly1015=
NM_001193640.2:c.2709C>T	NP_001180569.1:p.Gly903=
NM_001257965.2:c.2973C>T	NP_001244894.1:p.Gly991=
NR_047563.2:n.2998C>T
NR_047564.2:n.3206C>T
NM_001257966.2:c.2129-692C>T	NP_001244895.1:n.2129-692C>T