Canonical Allele Identifier: CA338848557
Gene: CDA HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.20944971G>C (hg19) chr1:g.20618478G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618478G>C , CM000663.2:g.20618478G>C GRCh38
NC_000001.10:g.20944971G>C , CM000663.1:g.20944971G>C GRCh37
NC_000001.9:g.20817558G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.351G>C MANE Select ENSP00000364212.3:p.Met117Ile
ENST00000375071.3:c.351G>C ENSP00000364212.3:p.Met117Ile
ENST00000461985.1:n.337G>C
NM_001785.2:c.351G>C NP_001776.1:p.Met117Ile
NM_001785.3:c.351G>C MANE Select NP_001776.1:p.Met117Ile
Search 100 bp 5'
Search 100 bp 3'