Canonical Allele Identifier: CA339866
Gene: DARS2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1061
dbSNP Id: rs121918208

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173831593G>T , CM000663.2:g.173831593G>T GRCh38
NC_000001.10:g.173800731G>T , CM000663.1:g.173800731G>T GRCh37
NC_000001.9:g.172067354G>T NCBI36
NG_016138.1:g.11935G>T

Transcript Alleles

HGVS Amino-acid change
NM_018122.4:c.455G>T VV NP_060592.2:p.Cys152Phe
XM_006711427.2:c.455G>T XP_006711490.1:p.Cys152Phe
XM_011509711.1:c.455G>T XP_011508013.1:p.Cys152Phe
NM_001365212.1:c.455G>T VV NP_001352141.1:p.Cys152Phe
NM_001365213.1:c.455G>T VV NP_001352142.1:p.Cys152Phe
NM_018122.5:c.455G>T VV NP_060592.2:p.Cys152Phe
ENST00000361951.4:c.455G>T ENSP00000355086.4:p.Cys152Phe