Canonical Allele Identifier: CA26854823
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs369205668
MyVariant Identifiers: chr1:g.94496512C>G (hg19) chr1:g.94030956C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030956C>G , CM000663.2:g.94030956C>G GRCh38
NC_000001.10:g.94496512C>G , CM000663.1:g.94496512C>G GRCh37
NC_000001.9:g.94269100C>G NCBI36
NG_009073.1:g.95194G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4253+40G>C MANE Select ENSP00000359245.3:n.4253+40G>C
ENST00000370225.3:c.4253+40G>C ENSP00000359245.3:n.4253+40G>C
ENST00000536513.5:c.629+40G>C ENSP00000439707.2:n.629+40G>C
NM_000350.2:c.4253+40G>C NP_000341.2:n.4253+40G>C
NM_000350.3:c.4253+40G>C MANE Select NP_000341.2:n.4253+40G>C
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