Canonical Allele Identifier: CA418826712
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94508953T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043397T>C , CM000663.2:g.94043397T>C GRCh38
NC_000001.10:g.94508953T>C , CM000663.1:g.94508953T>C GRCh37
NC_000001.9:g.94281541T>C NCBI36
NG_009073.1:g.82753A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3129A>G MANE Select ENSP00000359245.3:p.Glu1043=
ENST00000370225.3:c.3129A>G ENSP00000359245.3:p.Glu1043=
ENST00000536513.5:c.-64-3308A>G ENSP00000439707.2:n.-64-3308A>G
NM_000350.2:c.3129A>G NP_000341.2:p.Glu1043=
NM_000350.3:c.3129A>G MANE Select NP_000341.2:p.Glu1043=