Canonical Allele Identifier: CA418821535
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94526201C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060645C>T , CM000663.2:g.94060645C>T GRCh38
NC_000001.10:g.94526201C>T , CM000663.1:g.94526201C>T GRCh37
NC_000001.9:g.94298789C>T NCBI36
NG_009073.1:g.65505G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2052G>A MANE Select ENSP00000359245.3:p.Glu684=
ENST00000649773.1:c.2052G>A ENSP00000496882.1:p.Glu684=
ENST00000370225.3:c.2052G>A ENSP00000359245.3:p.Glu684=
ENST00000472033.1:n.172G>A
ENST00000536513.5:c.-65+2529G>A ENSP00000439707.2:n.-65+2529G>A
NM_000350.2:c.2052G>A NP_000341.2:p.Glu684=
NM_000350.3:c.2052G>A MANE Select NP_000341.2:p.Glu684=