Canonical Allele Identifier: CA26840906
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 929304
ClinVar RCV Id: RCV001270179 RCV002561021
dbSNP Id: rs985690206
gnomAD v2: 1-94512614-G-A
gnomAD v4: 1-94047058-G-A
MyVariant Identifiers: chr1:g.94512614G>A (hg19) chr1:g.94047058G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047058G>A , CM000663.2:g.94047058G>A GRCh38
NC_000001.10:g.94512614G>A , CM000663.1:g.94512614G>A GRCh37
NC_000001.9:g.94285202G>A NCBI36
NG_009073.1:g.79092C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2779C>T MANE Select ENSP00000359245.3:p.Pro927Ser
ENST00000649773.1:c.2557C>T ENSP00000496882.1:p.Pro853Ser
ENST00000370225.3:c.2779C>T ENSP00000359245.3:p.Pro927Ser
ENST00000536513.5:c.-64-6969C>T ENSP00000439707.2:n.-64-6969C>T
NM_000350.2:c.2779C>T NP_000341.2:p.Pro927Ser
NM_000350.3:c.2779C>T MANE Select NP_000341.2:p.Pro927Ser
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