Canonical Allele Identifier: CA1004553077
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1659882038
gnomAD v3: 1-94021078-G-A
gnomAD v4: 1-94021078-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021078G>A , CM000663.2:g.94021078G>A GRCh38
NC_000001.10:g.94486634G>A , CM000663.1:g.94486634G>A GRCh37
NC_000001.9:g.94259222G>A NCBI36
NG_009073.1:g.105072C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5018+162C>T MANE Select ENSP00000359245.3:n.5018+162C>T
ENST00000370225.3:c.5018+162C>T ENSP00000359245.3:n.5018+162C>T
ENST00000460514.1:n.512+162C>T
ENST00000470771.1:n.128+162C>T
ENST00000536513.5:c.1394+162C>T ENSP00000439707.2:n.1394+162C>T
NM_000350.2:c.5018+162C>T NP_000341.2:n.5018+162C>T
NM_000350.3:c.5018+162C>T MANE Select NP_000341.2:n.5018+162C>T