Canonical Allele Identifier: CA344032846

Gene: CRB1

Linked Data

• ClinVar Variation Id: 636167
• ClinVar RCV Id: RCV000787827
• dbSNP Id: rs1571525390
• MyVariant Identifiers: chr1:g.197390851T>G (hg19) ; chr1:g.197421721T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421721T>G , CM000663.2:g.197421721T>G	GRCh38
NC_000001.10:g.197390851T>G , CM000663.1:g.197390851T>G	GRCh37
NC_000001.9:g.195657474T>G	NCBI36
NG_008483.1:g.158444T>G
NG_008483.2:g.225260T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1893T>G MANE Select	ENSP00000356370.3:p.Tyr631Ter
ENST00000638467.1:c.1893T>G	ENSP00000491102.1:p.Tyr631Ter
ENST00000681519.1:c.774T>G	ENSP00000505267.1:p.Tyr258Ter
ENST00000367397.1:c.36T>G	ENSP00000356367.1:p.Tyr12Ter
ENST00000367399.6:c.1557T>G	ENSP00000356369.2:p.Tyr519Ter
ENST00000367400.7:c.1893T>G	ENSP00000356370.3:p.Tyr631Ter
ENST00000484075.5:c.1893T>G	ENSP00000433932.1:p.Tyr631Ter
ENST00000535699.5:c.1686T>G	ENSP00000438786.1:p.Tyr562Ter
ENST00000538660.5:c.1893T>G	ENSP00000438091.1:p.Tyr631Ter
NM_001193640.1:c.1557T>G	NP_001180569.1:p.Tyr519Ter
NM_001257965.1:c.1686T>G	NP_001244894.1:p.Tyr562Ter
NM_001257966.1:c.1893T>G	NP_001244895.1:p.Tyr631Ter
NM_201253.2:c.1893T>G	NP_957705.1:p.Tyr631Ter
NR_047563.1:n.1923-29T>G
NR_047564.1:n.2102T>G
XM_011509365.1:c.1893T>G	XP_011507667.1:p.Tyr631Ter
XM_011509366.1:c.1893T>G	XP_011507668.1:p.Tyr631Ter
XM_011509367.1:c.1893T>G	XP_011507669.1:p.Tyr631Ter
XM_011509368.1:c.1311T>G	XP_011507670.1:p.Tyr437Ter
XM_011509369.1:c.336T>G	XP_011507671.1:p.Tyr112Ter
XM_011509365.2:c.1893T>G	XP_011507667.1:p.Tyr631Ter
XM_011509369.2:c.336T>G	XP_011507671.1:p.Tyr112Ter
XM_017000851.1:c.1050T>G	XP_016856340.1:p.Tyr350Ter
XM_017000852.1:c.1893T>G	XP_016856341.1:p.Tyr631Ter
NM_201253.3:c.1893T>G MANE Select	NP_957705.1:p.Tyr631Ter
NM_001193640.2:c.1557T>G	NP_001180569.1:p.Tyr519Ter
NM_001257965.2:c.1686T>G	NP_001244894.1:p.Tyr562Ter
NR_047563.2:n.1875-29T>G
NR_047564.2:n.2054T>G
NM_001257966.2:c.1893T>G	NP_001244895.1:p.Tyr631Ter