Canonical Allele Identifier: CA524386126
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1269116642
gnomAD v2: 1-94526029-C-T
gnomAD v3: 1-94060473-C-T
gnomAD v4: 1-94060473-C-T
MyVariant Identifiers: chr1:g.94526029C>T (hg19) chr1:g.94060473C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060473C>T , CM000663.2:g.94060473C>T GRCh38
NC_000001.10:g.94526029C>T , CM000663.1:g.94526029C>T GRCh37
NC_000001.9:g.94298617C>T NCBI36
NG_009073.1:g.65677G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2160+64G>A MANE Select ENSP00000359245.3:n.2160+64G>A
ENST00000649773.1:c.2160+64G>A ENSP00000496882.1:n.2160+64G>A
ENST00000370225.3:c.2160+64G>A ENSP00000359245.3:n.2160+64G>A
ENST00000472033.1:n.280+64G>A
ENST00000536513.5:c.-65+2701G>A ENSP00000439707.2:n.-65+2701G>A
NM_000350.2:c.2160+64G>A NP_000341.2:n.2160+64G>A
NM_000350.3:c.2160+64G>A MANE Select NP_000341.2:n.2160+64G>A
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