Canonical Allele Identifier: CA660322
Gene: CDA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1048977

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_001785.2:c.435C>T VV NP_001776.1:p.Thr145=
NM_001785.3:c.435C>T VV MANE Preferred
ENST00000375071.3:c.435C>T ENSP00000364212.3:p.Thr145=
ENST00000461985.1:n.421C>T