Canonical Allele Identifier: CA1157639578
Gene: CDA HGNC NCBI

Linked Data

dbSNP Id: rs2052838421
gnomAD v4: 1-20618391-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618391A>C , CM000663.2:g.20618391A>C GRCh38
NC_000001.10:g.20944884A>C , CM000663.1:g.20944884A>C GRCh37
NC_000001.9:g.20817471A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-61A>C MANE Select ENSP00000364212.3:n.325-61A>C
ENST00000375071.3:c.325-61A>C ENSP00000364212.3:n.325-61A>C
ENST00000461985.1:n.311-61A>C
NM_001785.2:c.325-61A>C NP_001776.1:n.325-61A>C
NM_001785.3:c.325-61A>C MANE Select NP_001776.1:n.325-61A>C
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