Canonical Allele Identifier: CA1004554635
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1037075695
gnomAD v3: 1-94067472-G-A
gnomAD v4: 1-94067472-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94067472G>A , CM000663.2:g.94067472G>A GRCh38
NC_000001.10:g.94533028G>A , CM000663.1:g.94533028G>A GRCh37
NC_000001.9:g.94305616G>A NCBI36
NG_009073.1:g.58678C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1555-4155C>T MANE Select ENSP00000359245.3:n.1555-4155C>T
ENST00000649773.1:c.1555-4155C>T ENSP00000496882.1:n.1555-4155C>T
ENST00000370225.3:c.1555-4155C>T ENSP00000359245.3:n.1555-4155C>T
NM_000350.2:c.1555-4155C>T NP_000341.2:n.1555-4155C>T
NM_000350.3:c.1555-4155C>T MANE Select NP_000341.2:n.1555-4155C>T