Canonical Allele Identifier: CA2646647426
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94021602-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021602T>A , CM000663.2:g.94021602T>A GRCh38
NC_000001.10:g.94487158T>A , CM000663.1:g.94487158T>A GRCh37
NC_000001.9:g.94259746T>A NCBI36
NG_009073.1:g.104548A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4848+38A>T MANE Select ENSP00000359245.3:n.4848+38A>T
ENST00000370225.3:c.4848+38A>T ENSP00000359245.3:n.4848+38A>T
ENST00000460514.1:n.342+38A>T
ENST00000536513.5:c.1224+38A>T ENSP00000439707.2:n.1224+38A>T
NM_000350.2:c.4848+38A>T NP_000341.2:n.4848+38A>T
NM_000350.3:c.4848+38A>T MANE Select NP_000341.2:n.4848+38A>T