Canonical Allele Identifier: CA957956

Gene: ABCA4

Linked Data

• ClinVar Variation Id: 961495
• ClinVar RCV Id: RCV001235193
• dbSNP Id: rs369440533
• ExAC: 1:94506935 G / A
• gnomAD v2: 1-94506935-G-A
• gnomAD v3: 1-94041379-G-A
• gnomAD v4: 1-94041379-G-A
• MyVariant Identifiers: chr1:g.94506935G>A (hg19) ; chr1:g.94041379G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94041379G>A , CM000663.2:g.94041379G>A	GRCh38
NC_000001.10:g.94506935G>A , CM000663.1:g.94506935G>A	GRCh37
NC_000001.9:g.94279523G>A	NCBI36
NG_009073.1:g.84771C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.3352C>T MANE Select	ENSP00000359245.3:p.His1118Tyr
ENST00000370225.3:c.3352C>T	ENSP00000359245.3:p.His1118Tyr
ENST00000536513.5:c.-64-1290C>T	ENSP00000439707.2:n.-64-1290C>T
NM_000350.2:c.3352C>T	NP_000341.2:p.His1118Tyr
NM_000350.3:c.3352C>T MANE Select	NP_000341.2:p.His1118Tyr