Canonical Allele Identifier: CA26844688
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs370994559
gnomAD v3: 1-94021070-T-G
gnomAD v4: 1-94021070-T-G
MyVariant Identifiers: chr1:g.94486626T>G (hg19) chr1:g.94021070T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021070T>G , CM000663.2:g.94021070T>G GRCh38
NC_000001.10:g.94486626T>G , CM000663.1:g.94486626T>G GRCh37
NC_000001.9:g.94259214T>G NCBI36
NG_009073.1:g.105080A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5018+170A>C MANE Select ENSP00000359245.3:n.5018+170A>C
ENST00000370225.3:c.5018+170A>C ENSP00000359245.3:n.5018+170A>C
ENST00000460514.1:n.512+170A>C
ENST00000470771.1:n.128+170A>C
ENST00000536513.5:c.1394+170A>C ENSP00000439707.2:n.1394+170A>C
NM_000350.2:c.5018+170A>C NP_000341.2:n.5018+170A>C
NM_000350.3:c.5018+170A>C MANE Select NP_000341.2:n.5018+170A>C
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