Canonical Allele Identifier: CA35907397

Gene: CRB1

Linked Data

• dbSNP Id: rs954823148
• gnomAD v3: 1-197435173-G-A
• gnomAD v4: 1-197435173-G-A
• MyVariant Identifiers: chr1:g.197404303G>A (hg19) ; chr1:g.197435173G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435173G>A , CM000663.2:g.197435173G>A	GRCh38
NC_000001.10:g.197404303G>A , CM000663.1:g.197404303G>A	GRCh37
NC_000001.9:g.195670926G>A	NCBI36
NG_008483.1:g.171896G>A
NG_008483.2:g.238712G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.3310G>A MANE Select	ENSP00000356370.3:p.Gly1104Ser
ENST00000638467.1:c.3310G>A	ENSP00000491102.1:p.Gly1104Ser
ENST00000681519.1:c.2191G>A	ENSP00000505267.1:p.Gly731Ser
ENST00000367397.1:c.1453G>A	ENSP00000356367.1:p.Gly485Ser
ENST00000367399.6:c.2974G>A	ENSP00000356369.2:p.Gly992Ser
ENST00000367400.7:c.3310G>A	ENSP00000356370.3:p.Gly1104Ser
ENST00000484075.5:c.3310G>A	ENSP00000433932.1:p.Gly1104Ser
ENST00000535699.5:c.3238G>A	ENSP00000438786.1:p.Gly1080Ser
ENST00000538660.5:c.2129-427G>A	ENSP00000438091.1:n.2129-427G>A
NM_001193640.1:c.2974G>A	NP_001180569.1:p.Gly992Ser
NM_001257965.1:c.3238G>A	NP_001244894.1:p.Gly1080Ser
NM_001257966.1:c.2129-427G>A	NP_001244895.1:n.2129-427G>A
NM_201253.2:c.3310G>A	NP_957705.1:p.Gly1104Ser
NR_047563.1:n.3311G>A
NR_047564.1:n.3519G>A
XM_011509365.1:c.3310G>A	XP_011507667.1:p.Gly1104Ser
XM_011509366.1:c.3310G>A	XP_011507668.1:p.Gly1104Ser
XM_011509367.1:c.3310G>A	XP_011507669.1:p.Gly1104Ser
XM_011509368.1:c.2728G>A	XP_011507670.1:p.Gly910Ser
XM_011509369.1:c.1753G>A	XP_011507671.1:p.Gly585Ser
XM_011509365.2:c.3310G>A	XP_011507667.1:p.Gly1104Ser
XM_011509369.2:c.1753G>A	XP_011507671.1:p.Gly585Ser
XM_017000851.1:c.2467G>A	XP_016856340.1:p.Gly823Ser
XM_017000852.1:c.3445G>A	XP_016856341.1:p.Gly1149Ser
NM_201253.3:c.3310G>A MANE Select	NP_957705.1:p.Gly1104Ser
NM_001193640.2:c.2974G>A	NP_001180569.1:p.Gly992Ser
NM_001257965.2:c.3238G>A	NP_001244894.1:p.Gly1080Ser
NR_047563.2:n.3263G>A
NR_047564.2:n.3471G>A
NM_001257966.2:c.2129-427G>A	NP_001244895.1:n.2129-427G>A