Canonical Allele Identifier: CA26845008
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs889448722
gnomAD v2: 1-94487216-C-T
gnomAD v3: 1-94021660-C-T
gnomAD v4: 1-94021660-C-T
MyVariant Identifiers: chr1:g.94487216C>T (hg19) chr1:g.94021660C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021660C>T , CM000663.2:g.94021660C>T GRCh38
NC_000001.10:g.94487216C>T , CM000663.1:g.94487216C>T GRCh37
NC_000001.9:g.94259804C>T NCBI36
NG_009073.1:g.104490G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4828G>A MANE Select ENSP00000359245.3:p.Glu1610Lys
ENST00000370225.3:c.4828G>A ENSP00000359245.3:p.Glu1610Lys
ENST00000460514.1:n.322G>A
ENST00000536513.5:c.1204G>A ENSP00000439707.2:p.Glu402Lys
NM_000350.2:c.4828G>A NP_000341.2:p.Glu1610Lys
NM_000350.3:c.4828G>A MANE Select NP_000341.2:p.Glu1610Lys
Search 100 bp 5'
Search 100 bp 3'