Canonical Allele Identifier: CA418819832
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94481339A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015783A>T , CM000663.2:g.94015783A>T GRCh38
NC_000001.10:g.94481339A>T , CM000663.1:g.94481339A>T GRCh37
NC_000001.9:g.94253927A>T NCBI36
NG_009073.1:g.110367T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5268T>A MANE Select ENSP00000359245.3:p.Ser1756=
ENST00000370225.3:c.5268T>A ENSP00000359245.3:p.Ser1756=
ENST00000536513.5:c.1644T>A ENSP00000439707.2:p.Ser548=
NM_000350.2:c.5268T>A NP_000341.2:p.Ser1756=
NM_000350.3:c.5268T>A MANE Select NP_000341.2:p.Ser1756=