Canonical Allele Identifier: CA418825212
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2113838
ClinVar RCV Id: RCV003038979
dbSNP Id: rs2101036799
MyVariant Identifiers: chr1:g.94497361G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94031805G>A , CM000663.2:g.94031805G>A GRCh38
NC_000001.10:g.94497361G>A , CM000663.1:g.94497361G>A GRCh37
NC_000001.9:g.94269949G>A NCBI36
NG_009073.1:g.94345C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4101C>T MANE Select ENSP00000359245.3:p.Ile1367=
ENST00000370225.3:c.4101C>T ENSP00000359245.3:p.Ile1367=
ENST00000536513.5:c.477C>T ENSP00000439707.2:p.Ile159=
NM_000350.2:c.4101C>T NP_000341.2:p.Ile1367=
NM_000350.3:c.4101C>T MANE Select NP_000341.2:p.Ile1367=
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