Canonical Allele Identifier: CA957486
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs763146508
ExAC: 1:94487398 A / G
gnomAD v2: 1-94487398-A-G
gnomAD v3: 1-94021842-A-G
gnomAD v4: 1-94021842-A-G
MyVariant Identifiers: chr1:g.94487398A>G (hg19) chr1:g.94021842A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021842A>G , CM000663.2:g.94021842A>G GRCh38
NC_000001.10:g.94487398A>G , CM000663.1:g.94487398A>G GRCh37
NC_000001.9:g.94259986A>G NCBI36
NG_009073.1:g.104308T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4773+4T>C MANE Select ENSP00000359245.3:n.4773+4T>C
ENST00000370225.3:c.4773+4T>C ENSP00000359245.3:n.4773+4T>C
ENST00000460514.1:n.267+4T>C
ENST00000536513.5:c.1149+4T>C ENSP00000439707.2:n.1149+4T>C
NM_000350.2:c.4773+4T>C NP_000341.2:n.4773+4T>C
NM_000350.3:c.4773+4T>C MANE Select NP_000341.2:n.4773+4T>C
Search 100 bp 5'
Search 100 bp 3'