Canonical Allele Identifier: CA2643867541
Gene: CDA HGNC NCBI

Linked Data

gnomAD v4: 1-20618390-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618390C>A , CM000663.2:g.20618390C>A GRCh38
NC_000001.10:g.20944883C>A , CM000663.1:g.20944883C>A GRCh37
NC_000001.9:g.20817470C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-62C>A MANE Select ENSP00000364212.3:n.325-62C>A
ENST00000375071.3:c.325-62C>A ENSP00000364212.3:n.325-62C>A
ENST00000461985.1:n.311-62C>A
NM_001785.2:c.325-62C>A NP_001776.1:n.325-62C>A
NM_001785.3:c.325-62C>A MANE Select NP_001776.1:n.325-62C>A
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