Canonical Allele Identifier: CA341281589
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94481317C>T (hg19) chr1:g.94015761C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015761C>T , CM000663.2:g.94015761C>T GRCh38
NC_000001.10:g.94481317C>T , CM000663.1:g.94481317C>T GRCh37
NC_000001.9:g.94253905C>T NCBI36
NG_009073.1:g.110389G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5290G>A MANE Select ENSP00000359245.3:p.Val1764Met
ENST00000370225.3:c.5290G>A ENSP00000359245.3:p.Val1764Met
ENST00000536513.5:c.1666G>A ENSP00000439707.2:p.Val556Met
NM_000350.2:c.5290G>A NP_000341.2:p.Val1764Met
NM_000350.3:c.5290G>A MANE Select NP_000341.2:p.Val1764Met
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