Canonical Allele Identifier: CA2646650050
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94043530-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043530G>T , CM000663.2:g.94043530G>T GRCh38
NC_000001.10:g.94509086G>T , CM000663.1:g.94509086G>T GRCh37
NC_000001.9:g.94281674G>T NCBI36
NG_009073.1:g.82620C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3051-55C>A MANE Select ENSP00000359245.3:n.3051-55C>A
ENST00000370225.3:c.3051-55C>A ENSP00000359245.3:n.3051-55C>A
ENST00000536513.5:c.-64-3441C>A ENSP00000439707.2:n.-64-3441C>A
NM_000350.2:c.3051-55C>A NP_000341.2:n.3051-55C>A
NM_000350.3:c.3051-55C>A MANE Select NP_000341.2:n.3051-55C>A
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