Canonical Allele Identifier: CA418819689
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94015747-C-G
MyVariant Identifiers: chr1:g.94481303C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015747C>G , CM000663.2:g.94015747C>G GRCh38
NC_000001.10:g.94481303C>G , CM000663.1:g.94481303C>G GRCh37
NC_000001.9:g.94253891C>G NCBI36
NG_009073.1:g.110403G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5304G>C MANE Select ENSP00000359245.3:p.Leu1768=
ENST00000370225.3:c.5304G>C ENSP00000359245.3:p.Leu1768=
ENST00000536513.5:c.1680G>C ENSP00000439707.2:p.Leu560=
NM_000350.2:c.5304G>C NP_000341.2:p.Leu1768=
NM_000350.3:c.5304G>C MANE Select NP_000341.2:p.Leu1768=