Canonical Allele Identifier: CA2646645435
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94001839-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94001839G>C , CM000663.2:g.94001839G>C GRCh38
NC_000001.10:g.94467395G>C , CM000663.1:g.94467395G>C GRCh37
NC_000001.9:g.94239983G>C NCBI36
NG_009073.1:g.124311C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6282+19C>G MANE Select ENSP00000359245.3:n.6282+19C>G
ENST00000370225.3:c.6282+19C>G ENSP00000359245.3:n.6282+19C>G
ENST00000465352.1:n.717C>G
ENST00000536513.5:c.2658+19C>G ENSP00000439707.2:n.2658+19C>G
NM_000350.2:c.6282+19C>G NP_000341.2:n.6282+19C>G
NM_000350.3:c.6282+19C>G MANE Select NP_000341.2:n.6282+19C>G