Canonical Allele Identifier: CA341281050
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94011304-G-C
MyVariant Identifiers: chr1:g.94476860G>C (hg19) chr1:g.94011304G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94011304G>C , CM000663.2:g.94011304G>C GRCh38
NC_000001.10:g.94476860G>C , CM000663.1:g.94476860G>C GRCh37
NC_000001.9:g.94249448G>C NCBI36
NG_009073.1:g.114846C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5542C>G MANE Select ENSP00000359245.3:p.Leu1848Val
ENST00000370225.3:c.5542C>G ENSP00000359245.3:p.Leu1848Val
ENST00000536513.5:c.1918C>G ENSP00000439707.2:p.Leu640Val
NM_000350.2:c.5542C>G NP_000341.2:p.Leu1848Val
NM_000350.3:c.5542C>G MANE Select NP_000341.2:p.Leu1848Val
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