Canonical Allele Identifier: CA957249
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs772420273
gnomAD v2: 1-94476975-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94011419G>C , CM000663.2:g.94011419G>C GRCh38
NC_000001.10:g.94476975G>C , CM000663.1:g.94476975G>C GRCh37
NC_000001.9:g.94249563G>C NCBI36
NG_009073.1:g.114731C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.5461-34C>G MANE Select ENSP00000359245.3:n.5461-34C>G
ENST00000370225.3:c.5461-34C>G ENSP00000359245.3:n.5461-34C>G
ENST00000536513.5:c.1837-34C>G ENSP00000439707.2:n.1837-34C>G
NM_000350.2:c.5461-34C>G NP_000341.2:n.5461-34C>G
NM_000350.3:c.5461-34C>G MANE Select NP_000341.2:n.5461-34C>G