Canonical Allele Identifier: CA338848349

Gene: CDA

Linked Data

• MyVariant Identifiers: chr1:g.20944957T>G (hg19) ; chr1:g.20618464T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.20618464T>G , CM000663.2:g.20618464T>G	GRCh38
NC_000001.10:g.20944957T>G , CM000663.1:g.20944957T>G	GRCh37
NC_000001.9:g.20817544T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375071.4:c.337T>G MANE Select	ENSP00000364212.3:p.Trp113Gly
ENST00000375071.3:c.337T>G	ENSP00000364212.3:p.Trp113Gly
ENST00000461985.1:n.323T>G
NM_001785.2:c.337T>G	NP_001776.1:p.Trp113Gly
NM_001785.3:c.337T>G MANE Select	NP_001776.1:p.Trp113Gly