Canonical Allele Identifier: CA26848387
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs899890156
MyVariant Identifiers: chr1:g.94528394A>G (hg19) chr1:g.94062838A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062838A>G , CM000663.2:g.94062838A>G GRCh38
NC_000001.10:g.94528394A>G , CM000663.1:g.94528394A>G GRCh37
NC_000001.9:g.94300982A>G NCBI36
NG_009073.1:g.63312T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1761-85T>C MANE Select ENSP00000359245.3:n.1761-85T>C
ENST00000649773.1:c.1761-85T>C ENSP00000496882.1:n.1761-85T>C
ENST00000370225.3:c.1761-85T>C ENSP00000359245.3:n.1761-85T>C
ENST00000536513.5:c.-65+336T>C ENSP00000439707.2:n.-65+336T>C
NM_000350.2:c.1761-85T>C NP_000341.2:n.1761-85T>C
NM_000350.3:c.1761-85T>C MANE Select NP_000341.2:n.1761-85T>C
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