Canonical Allele Identifier: CA26851964
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1028892221
gnomAD v2: 1-94533180-T-C
gnomAD v3: 1-94067624-T-C
gnomAD v4: 1-94067624-T-C
MyVariant Identifiers: chr1:g.94533180T>C (hg19) chr1:g.94067624T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94067624T>C , CM000663.2:g.94067624T>C GRCh38
NC_000001.10:g.94533180T>C , CM000663.1:g.94533180T>C GRCh37
NC_000001.9:g.94305768T>C NCBI36
NG_009073.1:g.58526A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1555-4307A>G MANE Select ENSP00000359245.3:n.1555-4307A>G
ENST00000649773.1:c.1555-4307A>G ENSP00000496882.1:n.1555-4307A>G
ENST00000370225.3:c.1555-4307A>G ENSP00000359245.3:n.1555-4307A>G
NM_000350.2:c.1555-4307A>G NP_000341.2:n.1555-4307A>G
NM_000350.3:c.1555-4307A>G MANE Select NP_000341.2:n.1555-4307A>G
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