Canonical Allele Identifier: CA26844678
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs139366759
gnomAD v2: 1-94486599-T-C
gnomAD v3: 1-94021043-T-C
gnomAD v4: 1-94021043-T-C
MyVariant Identifiers: chr1:g.94486599T>C (hg19) chr1:g.94021043T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021043T>C , CM000663.2:g.94021043T>C GRCh38
NC_000001.10:g.94486599T>C , CM000663.1:g.94486599T>C GRCh37
NC_000001.9:g.94259187T>C NCBI36
NG_009073.1:g.105107A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5018+197A>G MANE Select ENSP00000359245.3:n.5018+197A>G
ENST00000370225.3:c.5018+197A>G ENSP00000359245.3:n.5018+197A>G
ENST00000460514.1:n.512+197A>G
ENST00000470771.1:n.128+197A>G
ENST00000536513.5:c.1394+197A>G ENSP00000439707.2:n.1394+197A>G
NM_000350.2:c.5018+197A>G NP_000341.2:n.5018+197A>G
NM_000350.3:c.5018+197A>G MANE Select NP_000341.2:n.5018+197A>G
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