Canonical Allele Identifier: CA740494821
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1412584578
gnomAD v3: 1-94030683-C-T
gnomAD v4: 1-94030683-C-T
MyVariant Identifiers: chr1:g.94496239C>T (hg19) chr1:g.94030683C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030683C>T , CM000663.2:g.94030683C>T GRCh38
NC_000001.10:g.94496239C>T , CM000663.1:g.94496239C>T GRCh37
NC_000001.9:g.94268827C>T NCBI36
NG_009073.1:g.95467G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4254-157G>A MANE Select ENSP00000359245.3:n.4254-157G>A
ENST00000370225.3:c.4254-157G>A ENSP00000359245.3:n.4254-157G>A
ENST00000536513.5:c.630-157G>A ENSP00000439707.2:n.630-157G>A
NM_000350.2:c.4254-157G>A NP_000341.2:n.4254-157G>A
NM_000350.3:c.4254-157G>A MANE Select NP_000341.2:n.4254-157G>A
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