Canonical Allele Identifier: CA660304
Gene: CDA HGNC NCBI

Linked Data

dbSNP Id: rs780595709
gnomAD v2: 1-20944959-G-T
gnomAD v4: 1-20618466-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.20618466G>T , CM000663.2:g.20618466G>T GRCh38
NC_000001.10:g.20944959G>T , CM000663.1:g.20944959G>T GRCh37
NC_000001.9:g.20817546G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375071.4:c.339G>T MANE Select ENSP00000364212.3:p.Trp113Cys
ENST00000375071.3:c.339G>T ENSP00000364212.3:p.Trp113Cys
ENST00000461985.1:n.325G>T
NM_001785.2:c.339G>T NP_001776.1:p.Trp113Cys
NM_001785.3:c.339G>T MANE Select NP_001776.1:p.Trp113Cys