Canonical Allele Identifier: CA341275575
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1298430
ClinVar RCV Id: RCV001726760
dbSNP Id: rs2101057455
MyVariant Identifiers: chr1:g.94512623C>T (hg19) chr1:g.94047067C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047067C>T , CM000663.2:g.94047067C>T GRCh38
NC_000001.10:g.94512623C>T , CM000663.1:g.94512623C>T GRCh37
NC_000001.9:g.94285211C>T NCBI36
NG_009073.1:g.79083G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2770G>A MANE Select ENSP00000359245.3:p.Gly924Arg
ENST00000649773.1:c.2548G>A ENSP00000496882.1:p.Gly850Arg
ENST00000370225.3:c.2770G>A ENSP00000359245.3:p.Gly924Arg
ENST00000536513.5:c.-64-6978G>A ENSP00000439707.2:n.-64-6978G>A
NM_000350.2:c.2770G>A NP_000341.2:p.Gly924Arg
NM_000350.3:c.2770G>A MANE Select NP_000341.2:p.Gly924Arg
Search 100 bp 5'
Search 100 bp 3'