Canonical Allele Identifier: CA2643867616
Gene: CDA HGNC NCBI

Linked Data

gnomAD v4: 1-20618570-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618570A>G , CM000663.2:g.20618570A>G GRCh38
NC_000001.10:g.20945063A>G , CM000663.1:g.20945063A>G GRCh37
NC_000001.9:g.20817650A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.*2A>G MANE Select ENSP00000364212.3:n.*2A>G
ENST00000375071.3:c.*2A>G ENSP00000364212.3:n.*2A>G
ENST00000461985.1:n.429A>G
NM_001785.2:c.*2A>G NP_001776.1:n.*2A>G
NM_001785.3:c.*2A>G MANE Select NP_001776.1:n.*2A>G
Search 100 bp 5'
Search 100 bp 3'