Canonical Allele Identifier: CA1181422676
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1660709211

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94047131G>A , CM000663.2:g.94047131G>A GRCh38
NC_000001.10:g.94512687G>A , CM000663.1:g.94512687G>A GRCh37
NC_000001.9:g.94285275G>A NCBI36
NG_009073.1:g.79019C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2744-38C>T MANE Select ENSP00000359245.3:n.2744-38C>T
ENST00000649773.1:c.2522-38C>T ENSP00000496882.1:n.2522-38C>T
ENST00000370225.3:c.2744-38C>T ENSP00000359245.3:n.2744-38C>T
ENST00000536513.5:c.-64-7042C>T ENSP00000439707.2:n.-64-7042C>T
NM_000350.2:c.2744-38C>T NP_000341.2:n.2744-38C>T
NM_000350.3:c.2744-38C>T MANE Select NP_000341.2:n.2744-38C>T