Canonical Allele Identifier: CA2643867516
Gene: CDA HGNC NCBI

Linked Data

gnomAD v4: 1-20618371-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618371G>A , CM000663.2:g.20618371G>A GRCh38
NC_000001.10:g.20944864G>A , CM000663.1:g.20944864G>A GRCh37
NC_000001.9:g.20817451G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-81G>A MANE Select ENSP00000364212.3:n.325-81G>A
ENST00000375071.3:c.325-81G>A ENSP00000364212.3:n.325-81G>A
ENST00000461985.1:n.311-81G>A
NM_001785.2:c.325-81G>A NP_001776.1:n.325-81G>A
NM_001785.3:c.325-81G>A MANE Select NP_001776.1:n.325-81G>A
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