Canonical Allele Identifier: CA2643867547
Gene: CDA HGNC NCBI

Linked Data

gnomAD v4: 1-20618394-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618394C>G , CM000663.2:g.20618394C>G GRCh38
NC_000001.10:g.20944887C>G , CM000663.1:g.20944887C>G GRCh37
NC_000001.9:g.20817474C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-58C>G MANE Select ENSP00000364212.3:n.325-58C>G
ENST00000375071.3:c.325-58C>G ENSP00000364212.3:n.325-58C>G
ENST00000461985.1:n.311-58C>G
NM_001785.2:c.325-58C>G NP_001776.1:n.325-58C>G
NM_001785.3:c.325-58C>G MANE Select NP_001776.1:n.325-58C>G
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