Canonical Allele Identifier: CA524382523
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1169831821
gnomAD v2: 1-94467408-A-G
gnomAD v4: 1-94001852-A-G
MyVariant Identifiers: chr1:g.94467408A>G (hg19) chr1:g.94001852A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001852A>G , CM000663.2:g.94001852A>G GRCh38
NC_000001.10:g.94467408A>G , CM000663.1:g.94467408A>G GRCh37
NC_000001.9:g.94239996A>G NCBI36
NG_009073.1:g.124298T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6282+6T>C MANE Select ENSP00000359245.3:n.6282+6T>C
ENST00000370225.3:c.6282+6T>C ENSP00000359245.3:n.6282+6T>C
ENST00000465352.1:n.704T>C
ENST00000536513.5:c.2658+6T>C ENSP00000439707.2:n.2658+6T>C
NM_000350.2:c.6282+6T>C NP_000341.2:n.6282+6T>C
NM_000350.3:c.6282+6T>C MANE Select NP_000341.2:n.6282+6T>C
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