Canonical Allele Identifier: CA1004552867
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1661154146
gnomAD v3: 1-94062507-A-C
gnomAD v4: 1-94062507-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062507A>C , CM000663.2:g.94062507A>C GRCh38
NC_000001.10:g.94528063A>C , CM000663.1:g.94528063A>C GRCh37
NC_000001.9:g.94300651A>C NCBI36
NG_009073.1:g.63643T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.1937+70T>G MANE Select ENSP00000359245.3:n.1937+70T>G
ENST00000649773.1:c.1937+70T>G ENSP00000496882.1:n.1937+70T>G
ENST00000370225.3:c.1937+70T>G ENSP00000359245.3:n.1937+70T>G
ENST00000536513.5:c.-65+667T>G ENSP00000439707.2:n.-65+667T>G
NM_000350.2:c.1937+70T>G NP_000341.2:n.1937+70T>G
NM_000350.3:c.1937+70T>G MANE Select NP_000341.2:n.1937+70T>G