Canonical Allele Identifier: CA341284773
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 857006
ClinVar RCV Id: RCV001062597
dbSNP Id: rs886046564
gnomAD v4: 1-94029452-G-C
MyVariant Identifiers: chr1:g.94495008G>C (hg19) chr1:g.94029452G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94029452G>C , CM000663.2:g.94029452G>C GRCh38
NC_000001.10:g.94495008G>C , CM000663.1:g.94495008G>C GRCh37
NC_000001.9:g.94267596G>C NCBI36
NG_009073.1:g.96698C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4532C>G MANE Select ENSP00000359245.3:p.Pro1511Arg
ENST00000370225.3:c.4532C>G ENSP00000359245.3:p.Pro1511Arg
ENST00000536513.5:c.908C>G ENSP00000439707.2:p.Pro303Arg
NM_000350.2:c.4532C>G NP_000341.2:p.Pro1511Arg
NM_000350.3:c.4532C>G MANE Select NP_000341.2:p.Pro1511Arg
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