Canonical Allele Identifier: CA1004550389
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v3: 1-94015699-T-C
gnomAD v4: 1-94015699-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94015699T>C , CM000663.2:g.94015699T>C GRCh38
NC_000001.10:g.94481255T>C , CM000663.1:g.94481255T>C GRCh37
NC_000001.9:g.94253843T>C NCBI36
NG_009073.1:g.110451A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.5312+40A>G MANE Select ENSP00000359245.3:n.5312+40A>G
ENST00000370225.3:c.5312+40A>G ENSP00000359245.3:n.5312+40A>G
ENST00000536513.5:c.1688+40A>G ENSP00000439707.2:n.1688+40A>G
NM_000350.2:c.5312+40A>G NP_000341.2:n.5312+40A>G
NM_000350.3:c.5312+40A>G MANE Select NP_000341.2:n.5312+40A>G