Canonical Allele Identifier: CA341285923
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1450732484
gnomAD v2: 1-94496071-G-T
gnomAD v4: 1-94030515-G-T
MyVariant Identifiers: chr1:g.94496071G>T (hg19) chr1:g.94030515G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030515G>T , CM000663.2:g.94030515G>T GRCh38
NC_000001.10:g.94496071G>T , CM000663.1:g.94496071G>T GRCh37
NC_000001.9:g.94268659G>T NCBI36
NG_009073.1:g.95635C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4265C>A MANE Select ENSP00000359245.3:p.Pro1422Gln
ENST00000370225.3:c.4265C>A ENSP00000359245.3:p.Pro1422Gln
ENST00000536513.5:c.641C>A ENSP00000439707.2:p.Pro214Gln
NM_000350.2:c.4265C>A NP_000341.2:p.Pro1422Gln
NM_000350.3:c.4265C>A MANE Select NP_000341.2:p.Pro1422Gln
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