Canonical Allele Identifier: CA418821632
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94526273C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060717C>T , CM000663.2:g.94060717C>T GRCh38
NC_000001.10:g.94526273C>T , CM000663.1:g.94526273C>T GRCh37
NC_000001.9:g.94298861C>T NCBI36
NG_009073.1:g.65433G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1980G>A MANE Select ENSP00000359245.3:p.Val660=
ENST00000649773.1:c.1980G>A ENSP00000496882.1:p.Val660=
ENST00000370225.3:c.1980G>A ENSP00000359245.3:p.Val660=
ENST00000472033.1:n.100G>A
ENST00000536513.5:c.-65+2457G>A ENSP00000439707.2:n.-65+2457G>A
NM_000350.2:c.1980G>A NP_000341.2:p.Val660=
NM_000350.3:c.1980G>A MANE Select NP_000341.2:p.Val660=
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