Canonical Allele Identifier: CA418819727
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2771904
ClinVar RCV Id: RCV003574490
MyVariant Identifiers: chr1:g.94481315C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015759C>A , CM000663.2:g.94015759C>A GRCh38
NC_000001.10:g.94481315C>A , CM000663.1:g.94481315C>A GRCh37
NC_000001.9:g.94253903C>A NCBI36
NG_009073.1:g.110391G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5292G>T MANE Select ENSP00000359245.3:p.Val1764=
ENST00000370225.3:c.5292G>T ENSP00000359245.3:p.Val1764=
ENST00000536513.5:c.1668G>T ENSP00000439707.2:p.Val556=
NM_000350.2:c.5292G>T NP_000341.2:p.Val1764=
NM_000350.3:c.5292G>T MANE Select NP_000341.2:p.Val1764=