Canonical Allele Identifier: CA1004570017
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1659050533
gnomAD v3: 1-93997842-T-G
gnomAD v4: 1-93997842-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997842T>G , CM000663.2:g.93997842T>G GRCh38
NC_000001.10:g.94463398T>G , CM000663.1:g.94463398T>G GRCh37
NC_000001.9:g.94235986T>G NCBI36
NG_009073.1:g.128308A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6729+19A>C MANE Select ENSP00000359245.3:n.6729+19A>C
ENST00000370225.3:c.6729+19A>C ENSP00000359245.3:n.6729+19A>C
ENST00000536513.5:c.3105+19A>C ENSP00000439707.2:n.3105+19A>C
NM_000350.2:c.6729+19A>C NP_000341.2:n.6729+19A>C
NM_000350.3:c.6729+19A>C MANE Select NP_000341.2:n.6729+19A>C