Canonical Allele Identifier: CA338848553
Gene: CDA HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.20944969A>T (hg19) chr1:g.20618476A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618476A>T , CM000663.2:g.20618476A>T GRCh38
NC_000001.10:g.20944969A>T , CM000663.1:g.20944969A>T GRCh37
NC_000001.9:g.20817556A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.349A>T MANE Select ENSP00000364212.3:p.Met117Leu
ENST00000375071.3:c.349A>T ENSP00000364212.3:p.Met117Leu
ENST00000461985.1:n.335A>T
NM_001785.2:c.349A>T NP_001776.1:p.Met117Leu
NM_001785.3:c.349A>T MANE Select NP_001776.1:p.Met117Leu
Search 100 bp 5'
Search 100 bp 3'