Canonical Allele Identifier: CA957140
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs767742255
ExAC: 1:94476187 A / G
gnomAD v2: 1-94476187-A-G
gnomAD v3: 1-94010631-A-G
gnomAD v4: 1-94010631-A-G
MyVariant Identifiers: chr1:g.94476187A>G (hg19) chr1:g.94010631A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94010631A>G , CM000663.2:g.94010631A>G GRCh38
NC_000001.10:g.94476187A>G , CM000663.1:g.94476187A>G GRCh37
NC_000001.9:g.94248775A>G NCBI36
NG_009073.1:g.115519T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5714+169T>C MANE Select ENSP00000359245.3:n.5714+169T>C
ENST00000370225.3:c.5714+169T>C ENSP00000359245.3:n.5714+169T>C
ENST00000465352.1:n.130+169T>C
ENST00000536513.5:c.2090+169T>C ENSP00000439707.2:n.2090+169T>C
NM_000350.2:c.5714+169T>C NP_000341.2:n.5714+169T>C
NM_000350.3:c.5714+169T>C MANE Select NP_000341.2:n.5714+169T>C
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