Canonical Allele Identifier: CA416488669
Gene: CDA HGNC NCBI

Linked Data

gnomAD v4: 1-20618562-C-A
MyVariant Identifiers: chr1:g.20945055C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618562C>A , CM000663.2:g.20618562C>A GRCh38
NC_000001.10:g.20945055C>A , CM000663.1:g.20945055C>A GRCh37
NC_000001.9:g.20817642C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.435C>A MANE Select ENSP00000364212.3:p.Thr145=
ENST00000375071.3:c.435C>A ENSP00000364212.3:p.Thr145=
ENST00000461985.1:n.421C>A
NM_001785.2:c.435C>A NP_001776.1:p.Thr145=
NM_001785.3:c.435C>A MANE Select NP_001776.1:p.Thr145=
Search 100 bp 5'
Search 100 bp 3'