Canonical Allele Identifier: CA341291378
Gene: ABCA4 HGNC NCBI

Linked Data

gnomAD v4: 1-94041397-T-C
MyVariant Identifiers: chr1:g.94506953T>C (hg19) chr1:g.94041397T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94041397T>C , CM000663.2:g.94041397T>C GRCh38
NC_000001.10:g.94506953T>C , CM000663.1:g.94506953T>C GRCh37
NC_000001.9:g.94279541T>C NCBI36
NG_009073.1:g.84753A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.3334A>G MANE Select ENSP00000359245.3:p.Thr1112Ala
ENST00000370225.3:c.3334A>G ENSP00000359245.3:p.Thr1112Ala
ENST00000536513.5:c.-64-1308A>G ENSP00000439707.2:n.-64-1308A>G
NM_000350.2:c.3334A>G NP_000341.2:p.Thr1112Ala
NM_000350.3:c.3334A>G MANE Select NP_000341.2:p.Thr1112Ala
Search 100 bp 5'
Search 100 bp 3'