Canonical Allele Identifier: CA524384885
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs987212130
gnomAD v2: 1-94577204-T-G
gnomAD v3: 1-94111648-T-G
gnomAD v4: 1-94111648-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94111648T>G , CM000663.2:g.94111648T>G GRCh38
NC_000001.10:g.94577204T>G , CM000663.1:g.94577204T>G GRCh37
NC_000001.9:g.94349792T>G NCBI36
NG_009073.1:g.14502A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.161-69A>C MANE Select ENSP00000359245.3:n.161-69A>C
ENST00000649773.1:c.161-69A>C ENSP00000496882.1:n.161-69A>C
ENST00000370225.3:c.161-69A>C ENSP00000359245.3:n.161-69A>C
NM_000350.2:c.161-69A>C NP_000341.2:n.161-69A>C
NM_000350.3:c.161-69A>C MANE Select NP_000341.2:n.161-69A>C