Canonical Allele Identifier: CA341292428
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509268
ClinVar RCV Id: RCV002017777
dbSNP Id: rs1265535267
gnomAD v2: 1-94508910-C-G
gnomAD v4: 1-94043354-C-G
MyVariant Identifiers: chr1:g.94508910C>G (hg19) chr1:g.94043354C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043354C>G , CM000663.2:g.94043354C>G GRCh38
NC_000001.10:g.94508910C>G , CM000663.1:g.94508910C>G GRCh37
NC_000001.9:g.94281498C>G NCBI36
NG_009073.1:g.82796G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3172G>C MANE Select ENSP00000359245.3:p.Glu1058Gln
ENST00000370225.3:c.3172G>C ENSP00000359245.3:p.Glu1058Gln
ENST00000536513.5:c.-64-3265G>C ENSP00000439707.2:n.-64-3265G>C
NM_000350.2:c.3172G>C NP_000341.2:p.Glu1058Gln
NM_000350.3:c.3172G>C MANE Select NP_000341.2:p.Glu1058Gln
Search 100 bp 5'
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