Canonical Allele Identifier: CA2696612815
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs2101078745

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062897T>A , CM000663.2:g.94062897T>A GRCh38
NC_000001.10:g.94528453T>A , CM000663.1:g.94528453T>A GRCh37
NC_000001.9:g.94301041T>A NCBI36
NG_009073.1:g.63253A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1761-144A>T MANE Select ENSP00000359245.3:n.1761-144A>T
ENST00000649773.1:c.1761-144A>T ENSP00000496882.1:n.1761-144A>T
ENST00000370225.3:c.1761-144A>T ENSP00000359245.3:n.1761-144A>T
ENST00000536513.5:c.-65+277A>T ENSP00000439707.2:n.-65+277A>T
NM_000350.2:c.1761-144A>T NP_000341.2:n.1761-144A>T
NM_000350.3:c.1761-144A>T MANE Select NP_000341.2:n.1761-144A>T