Canonical Allele Identifier: CA999352413
Gene: CDA HGNC NCBI

Linked Data

dbSNP Id: rs2052838437
gnomAD v3: 1-20618392-G-T
gnomAD v4: 1-20618392-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618392G>T , CM000663.2:g.20618392G>T GRCh38
NC_000001.10:g.20944885G>T , CM000663.1:g.20944885G>T GRCh37
NC_000001.9:g.20817472G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.325-60G>T MANE Select ENSP00000364212.3:n.325-60G>T
ENST00000375071.3:c.325-60G>T ENSP00000364212.3:n.325-60G>T
ENST00000461985.1:n.311-60G>T
NM_001785.2:c.325-60G>T NP_001776.1:n.325-60G>T
NM_001785.3:c.325-60G>T MANE Select NP_001776.1:n.325-60G>T
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Search 100 bp 3'