Canonical Allele Identifier: CA957662
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 813136
ClinVar RCV Id: RCV001199615
dbSNP Id: rs778456901
ExAC: 1:94496067 G / A
MyVariant Identifiers: chr1:g.94496067G>A (hg19) chr1:g.94030511G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030511G>A , CM000663.2:g.94030511G>A GRCh38
NC_000001.10:g.94496067G>A , CM000663.1:g.94496067G>A GRCh37
NC_000001.9:g.94268655G>A NCBI36
NG_009073.1:g.95639C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4269C>T MANE Select ENSP00000359245.3:p.Gly1423=
ENST00000370225.3:c.4269C>T ENSP00000359245.3:p.Gly1423=
ENST00000536513.5:c.645C>T ENSP00000439707.2:p.Gly215=
NM_000350.2:c.4269C>T NP_000341.2:p.Gly1423=
NM_000350.3:c.4269C>T MANE Select NP_000341.2:p.Gly1423=
Search 100 bp 5'
Search 100 bp 3'