Canonical Allele Identifier: CA338849345
Gene: CDA HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.20945061A>G (hg19) chr1:g.20618568A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618568A>G , CM000663.2:g.20618568A>G GRCh38
NC_000001.10:g.20945061A>G , CM000663.1:g.20945061A>G GRCh37
NC_000001.9:g.20817648A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.441A>G MANE Select ENSP00000364212.3:p.Ter147Trp
ENST00000375071.3:c.441A>G ENSP00000364212.3:p.Ter147Trp
ENST00000461985.1:n.427A>G
NM_001785.2:c.441A>G NP_001776.1:p.Ter147Trp
NM_001785.3:c.441A>G MANE Select NP_001776.1:p.Ter147Trp
Search 100 bp 5'
Search 100 bp 3'