Canonical Allele Identifier: CA1312005

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1131457
• ClinVar RCV Id: RCV001465345
• dbSNP Id: rs370486884
• ExAC: 1:197390905 T / C
• gnomAD v2: 1-197390905-T-C
• gnomAD v3: 1-197421775-T-C
• gnomAD v4: 1-197421775-T-C
• MyVariant Identifiers: chr1:g.197390905T>C (hg19) ; chr1:g.197421775T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421775T>C , CM000663.2:g.197421775T>C	GRCh38
NC_000001.10:g.197390905T>C , CM000663.1:g.197390905T>C	GRCh37
NC_000001.9:g.195657528T>C	NCBI36
NG_008483.1:g.158498T>C
NG_008483.2:g.225314T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1947T>C MANE Select	ENSP00000356370.3:p.Asp649=
ENST00000638467.1:c.1947T>C	ENSP00000491102.1:p.Asp649=
ENST00000681519.1:c.828T>C	ENSP00000505267.1:p.Asp276=
ENST00000367397.1:c.90T>C	ENSP00000356367.1:p.Asp30=
ENST00000367399.6:c.1611T>C	ENSP00000356369.2:p.Asp537=
ENST00000367400.7:c.1947T>C	ENSP00000356370.3:p.Asp649=
ENST00000484075.5:c.1947T>C	ENSP00000433932.1:p.Asp649=
ENST00000535699.5:c.1740T>C	ENSP00000438786.1:p.Asp580=
ENST00000538660.5:c.1947T>C	ENSP00000438091.1:p.Asp649=
NM_001193640.1:c.1611T>C	NP_001180569.1:p.Asp537=
NM_001257965.1:c.1740T>C	NP_001244894.1:p.Asp580=
NM_001257966.1:c.1947T>C	NP_001244895.1:p.Asp649=
NM_201253.2:c.1947T>C	NP_957705.1:p.Asp649=
NR_047563.1:n.1948T>C
NR_047564.1:n.2156T>C
XM_011509365.1:c.1947T>C	XP_011507667.1:p.Asp649=
XM_011509366.1:c.1947T>C	XP_011507668.1:p.Asp649=
XM_011509367.1:c.1947T>C	XP_011507669.1:p.Asp649=
XM_011509368.1:c.1365T>C	XP_011507670.1:p.Asp455=
XM_011509369.1:c.390T>C	XP_011507671.1:p.Asp130=
XM_011509365.2:c.1947T>C	XP_011507667.1:p.Asp649=
XM_011509369.2:c.390T>C	XP_011507671.1:p.Asp130=
XM_017000851.1:c.1104T>C	XP_016856340.1:p.Asp368=
XM_017000852.1:c.1947T>C	XP_016856341.1:p.Asp649=
NM_201253.3:c.1947T>C MANE Select	NP_957705.1:p.Asp649=
NM_001193640.2:c.1611T>C	NP_001180569.1:p.Asp537=
NM_001257965.2:c.1740T>C	NP_001244894.1:p.Asp580=
NR_047563.2:n.1900T>C
NR_047564.2:n.2108T>C
NM_001257966.2:c.1947T>C	NP_001244895.1:p.Asp649=