Canonical Allele Identifier: CA341283695
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 941050
ClinVar RCV Id: RCV001210757
dbSNP Id: rs1659903133
MyVariant Identifiers: chr1:g.94487261T>C (hg19) chr1:g.94021705T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021705T>C , CM000663.2:g.94021705T>C GRCh38
NC_000001.10:g.94487261T>C , CM000663.1:g.94487261T>C GRCh37
NC_000001.9:g.94259849T>C NCBI36
NG_009073.1:g.104445A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4783A>G MANE Select ENSP00000359245.3:p.Thr1595Ala
ENST00000370225.3:c.4783A>G ENSP00000359245.3:p.Thr1595Ala
ENST00000460514.1:n.277A>G
ENST00000536513.5:c.1159A>G ENSP00000439707.2:p.Thr387Ala
NM_000350.2:c.4783A>G NP_000341.2:p.Thr1595Ala
NM_000350.3:c.4783A>G MANE Select NP_000341.2:p.Thr1595Ala
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