Canonical Allele Identifier: CA341275639
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94512651T>G (hg19) chr1:g.94047095T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047095T>G , CM000663.2:g.94047095T>G GRCh38
NC_000001.10:g.94512651T>G , CM000663.1:g.94512651T>G GRCh37
NC_000001.9:g.94285239T>G NCBI36
NG_009073.1:g.79055A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2744-2A>C MANE Select ENSP00000359245.3:n.2744-2A>C
ENST00000649773.1:c.2522-2A>C ENSP00000496882.1:n.2522-2A>C
ENST00000370225.3:c.2744-2A>C ENSP00000359245.3:n.2744-2A>C
ENST00000536513.5:c.-64-7006A>C ENSP00000439707.2:n.-64-7006A>C
NM_000350.2:c.2744-2A>C NP_000341.2:n.2744-2A>C
NM_000350.3:c.2744-2A>C MANE Select NP_000341.2:n.2744-2A>C
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