Canonical Allele Identifier: CA956965
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs764107121
gnomAD v2: 1-94467373-A-G
gnomAD v4: 1-94001817-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001817A>G , CM000663.2:g.94001817A>G GRCh38
NC_000001.10:g.94467373A>G , CM000663.1:g.94467373A>G GRCh37
NC_000001.9:g.94239961A>G NCBI36
NG_009073.1:g.124333T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6282+41T>C MANE Select ENSP00000359245.3:n.6282+41T>C
ENST00000370225.3:c.6282+41T>C ENSP00000359245.3:n.6282+41T>C
ENST00000465352.1:n.739T>C
ENST00000536513.5:c.2658+41T>C ENSP00000439707.2:n.2658+41T>C
NM_000350.2:c.6282+41T>C NP_000341.2:n.6282+41T>C
NM_000350.3:c.6282+41T>C MANE Select NP_000341.2:n.6282+41T>C