Canonical Allele Identifier: CA2044693
Gene: MARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1962457
ClinVar RCV Id: RCV002726147
dbSNP Id: rs776237269

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706516C>T , CM000664.2:g.197706516C>T GRCh38
NC_000002.11:g.198571240C>T , CM000664.1:g.198571240C>T GRCh37
NC_000002.10:g.198279485C>T NCBI36
NG_034122.1:g.6213C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282276.8:c.1111C>T MANE Select ENSP00000282276.6:p.Arg371Cys
ENST00000282276.7:c.1111C>T ENSP00000282276.6:p.Arg371Cys
NM_138395.3:c.1111C>T NP_612404.1:p.Arg371Cys
NM_138395.4:c.1111C>T MANE Select NP_612404.1:p.Arg371Cys