Canonical Allele Identifier: CA2646650053
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94043549-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043549T>G , CM000663.2:g.94043549T>G GRCh38
NC_000001.10:g.94509105T>G , CM000663.1:g.94509105T>G GRCh37
NC_000001.9:g.94281693T>G NCBI36
NG_009073.1:g.82601A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3051-74A>C MANE Select ENSP00000359245.3:n.3051-74A>C
ENST00000370225.3:c.3051-74A>C ENSP00000359245.3:n.3051-74A>C
ENST00000536513.5:c.-64-3460A>C ENSP00000439707.2:n.-64-3460A>C
NM_000350.2:c.3051-74A>C NP_000341.2:n.3051-74A>C
NM_000350.3:c.3051-74A>C MANE Select NP_000341.2:n.3051-74A>C
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