Canonical Allele Identifier: CA26863767

Gene: ABCA4

Linked Data

• dbSNP Id: rs1047375
• MyVariant Identifiers: chr1:g.94506913A>T (hg19) ; chr1:g.94041357A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94041357A>T , CM000663.2:g.94041357A>T	GRCh38
NC_000001.10:g.94506913A>T , CM000663.1:g.94506913A>T	GRCh37
NC_000001.9:g.94279501A>T	NCBI36
NG_009073.1:g.84793T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.3374T>A MANE Select	ENSP00000359245.3:p.Leu1125His
ENST00000370225.3:c.3374T>A	ENSP00000359245.3:p.Leu1125His
ENST00000536513.5:c.-64-1268T>A	ENSP00000439707.2:n.-64-1268T>A
NM_000350.2:c.3374T>A	NP_000341.2:p.Leu1125His
NM_000350.3:c.3374T>A MANE Select	NP_000341.2:p.Leu1125His