Canonical Allele Identifier: CA660324
Gene: CDA HGNC NCBI

Linked Data

dbSNP Id: rs72650823
ExAC: 1:20945064 G / A
gnomAD v2: 1-20945064-G-A
gnomAD v3: 1-20618571-G-A
gnomAD v4: 1-20618571-G-A
MyVariant Identifiers: chr1:g.20945064G>A (hg19) chr1:g.20618571G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618571G>A , CM000663.2:g.20618571G>A GRCh38
NC_000001.10:g.20945064G>A , CM000663.1:g.20945064G>A GRCh37
NC_000001.9:g.20817651G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.*3G>A MANE Select ENSP00000364212.3:n.*3G>A
ENST00000375071.3:c.*3G>A ENSP00000364212.3:n.*3G>A
ENST00000461985.1:n.430G>A
NM_001785.2:c.*3G>A NP_001776.1:n.*3G>A
NM_001785.3:c.*3G>A MANE Select NP_001776.1:n.*3G>A
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Search 100 bp 3'