Canonical Allele Identifier: CA418821785
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94528141C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062585C>A , CM000663.2:g.94062585C>A GRCh38
NC_000001.10:g.94528141C>A , CM000663.1:g.94528141C>A GRCh37
NC_000001.9:g.94300729C>A NCBI36
NG_009073.1:g.63565G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.1929G>T MANE Select ENSP00000359245.3:p.Val643=
ENST00000649773.1:c.1929G>T ENSP00000496882.1:p.Val643=
ENST00000370225.3:c.1929G>T ENSP00000359245.3:p.Val643=
ENST00000536513.5:c.-65+589G>T ENSP00000439707.2:n.-65+589G>T
NM_000350.2:c.1929G>T NP_000341.2:p.Val643=
NM_000350.3:c.1929G>T MANE Select NP_000341.2:p.Val643=
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Search 100 bp 3'