Canonical Allele Identifier: CA524384471
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs1256867547
gnomAD v2: 1-94509083-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043527G>A , CM000663.2:g.94043527G>A GRCh38
NC_000001.10:g.94509083G>A , CM000663.1:g.94509083G>A GRCh37
NC_000001.9:g.94281671G>A NCBI36
NG_009073.1:g.82623C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3051-52C>T MANE Select ENSP00000359245.3:n.3051-52C>T
ENST00000370225.3:c.3051-52C>T ENSP00000359245.3:n.3051-52C>T
ENST00000536513.5:c.-64-3438C>T ENSP00000439707.2:n.-64-3438C>T
NM_000350.2:c.3051-52C>T NP_000341.2:n.3051-52C>T
NM_000350.3:c.3051-52C>T MANE Select NP_000341.2:n.3051-52C>T