Canonical Allele Identifier: CA259925
Gene: DARS2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 30863
ClinVar RCV Id: RCV000023848
dbSNP Id: rs200670286

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857592C>T , CM000663.2:g.173857592C>T GRCh38
NC_000001.10:g.173826730C>T , CM000663.1:g.173826730C>T GRCh37
NC_000001.9:g.172093353C>T NCBI36
NG_016138.1:g.37934C>T

Transcript Alleles

HGVS Amino-acid change
NM_018122.4:c.1825C>T VV NP_060592.2:p.Arg609Trp
XM_006711427.2:c.1672C>T XP_006711490.1:p.Arg558Trp
NM_001365212.1:c.1672C>T VV NP_001352141.1:p.Arg558Trp
NM_018122.5:c.1825C>T VV
ENST00000361951.4:c.1825C>T ENSP00000355086.4:p.Arg609Trp
ENST00000471476.1:n.647C>T