Canonical Allele Identifier: CA338848568
Gene: CDA HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.20944972A>C (hg19) chr1:g.20618479A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618479A>C , CM000663.2:g.20618479A>C GRCh38
NC_000001.10:g.20944972A>C , CM000663.1:g.20944972A>C GRCh37
NC_000001.9:g.20817559A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.352A>C MANE Select ENSP00000364212.3:p.Thr118Pro
ENST00000375071.3:c.352A>C ENSP00000364212.3:p.Thr118Pro
ENST00000461985.1:n.338A>C
NM_001785.2:c.352A>C NP_001776.1:p.Thr118Pro
NM_001785.3:c.352A>C MANE Select NP_001776.1:p.Thr118Pro
Search 100 bp 5'
Search 100 bp 3'