Canonical Allele Identifier: CA418822178
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94528266G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062710G>T , CM000663.2:g.94062710G>T GRCh38
NC_000001.10:g.94528266G>T , CM000663.1:g.94528266G>T GRCh37
NC_000001.9:g.94300854G>T NCBI36
NG_009073.1:g.63440C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1804C>A MANE Select ENSP00000359245.3:p.Arg602=
ENST00000649773.1:c.1804C>A ENSP00000496882.1:p.Arg602=
ENST00000370225.3:c.1804C>A ENSP00000359245.3:p.Arg602=
ENST00000536513.5:c.-65+464C>A ENSP00000439707.2:n.-65+464C>A
NM_000350.2:c.1804C>A NP_000341.2:p.Arg602=
NM_000350.3:c.1804C>A MANE Select NP_000341.2:p.Arg602=
Search 100 bp 5'
Search 100 bp 3'