Canonical Allele Identifier: CA26840689
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs979887312
gnomAD v3: 1-94046690-G-A
gnomAD v4: 1-94046690-G-A
MyVariant Identifiers: chr1:g.94512246G>A (hg19) chr1:g.94046690G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94046690G>A , CM000663.2:g.94046690G>A GRCh38
NC_000001.10:g.94512246G>A , CM000663.1:g.94512246G>A GRCh37
NC_000001.9:g.94284834G>A NCBI36
NG_009073.1:g.79460C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2918+229C>T MANE Select ENSP00000359245.3:n.2918+229C>T
ENST00000649773.1:c.2696+229C>T ENSP00000496882.1:n.2696+229C>T
ENST00000370225.3:c.2918+229C>T ENSP00000359245.3:n.2918+229C>T
ENST00000536513.5:c.-64-6601C>T ENSP00000439707.2:n.-64-6601C>T
NM_000350.2:c.2918+229C>T NP_000341.2:n.2918+229C>T
NM_000350.3:c.2918+229C>T MANE Select NP_000341.2:n.2918+229C>T
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