Canonical Allele Identifier: CA958336
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs778120372
ExAC: 1:94526058 T / C
gnomAD v2: 1-94526058-T-C
gnomAD v3: 1-94060502-T-C
gnomAD v4: 1-94060502-T-C
MyVariant Identifiers: chr1:g.94526058T>C (hg19) chr1:g.94060502T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060502T>C , CM000663.2:g.94060502T>C GRCh38
NC_000001.10:g.94526058T>C , CM000663.1:g.94526058T>C GRCh37
NC_000001.9:g.94298646T>C NCBI36
NG_009073.1:g.65648A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2160+35A>G MANE Select ENSP00000359245.3:n.2160+35A>G
ENST00000649773.1:c.2160+35A>G ENSP00000496882.1:n.2160+35A>G
ENST00000370225.3:c.2160+35A>G ENSP00000359245.3:n.2160+35A>G
ENST00000472033.1:n.280+35A>G
ENST00000536513.5:c.-65+2672A>G ENSP00000439707.2:n.-65+2672A>G
NM_000350.2:c.2160+35A>G NP_000341.2:n.2160+35A>G
NM_000350.3:c.2160+35A>G MANE Select NP_000341.2:n.2160+35A>G
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