Canonical Allele Identifier: CA350213572
Gene: MARS2 HGNC NCBI

Linked Data

dbSNP Id: rs1192243489

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706412G>A , CM000664.2:g.197706412G>A GRCh38
NC_000002.11:g.198571136G>A , CM000664.1:g.198571136G>A GRCh37
NC_000002.10:g.198279381G>A NCBI36
NG_034122.1:g.6109G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1007G>A MANE Select ENSP00000282276.6:p.Cys336Tyr
ENST00000282276.7:c.1007G>A ENSP00000282276.6:p.Cys336Tyr
NM_138395.3:c.1007G>A NP_612404.1:p.Cys336Tyr
NM_138395.4:c.1007G>A MANE Select NP_612404.1:p.Cys336Tyr