Canonical Allele Identifier: CA956962
Gene: ABCA4 HGNC NCBI

Linked Data

dbSNP Id: rs759182752
gnomAD v2: 1-94467365-G-A
gnomAD v3: 1-94001809-G-A
gnomAD v4: 1-94001809-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001809G>A , CM000663.2:g.94001809G>A GRCh38
NC_000001.10:g.94467365G>A , CM000663.1:g.94467365G>A GRCh37
NC_000001.9:g.94239953G>A NCBI36
NG_009073.1:g.124341C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6282+49C>T MANE Select ENSP00000359245.3:n.6282+49C>T
ENST00000370225.3:c.6282+49C>T ENSP00000359245.3:n.6282+49C>T
ENST00000465352.1:n.747C>T
ENST00000536513.5:c.2658+49C>T ENSP00000439707.2:n.2658+49C>T
NM_000350.2:c.6282+49C>T NP_000341.2:n.6282+49C>T
NM_000350.3:c.6282+49C>T MANE Select NP_000341.2:n.6282+49C>T