Canonical Allele Identifier: CA320245
Gene: MARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214629
ClinVar RCV Id: RCV000195863
dbSNP Id: rs146365382

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706499A>G , CM000664.2:g.197706499A>G GRCh38
NC_000002.11:g.198571223A>G , CM000664.1:g.198571223A>G GRCh37
NC_000002.10:g.198279468A>G NCBI36
NG_034122.1:g.6196A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1094A>G MANE Select ENSP00000282276.6:p.Tyr365Cys
ENST00000282276.7:c.1094A>G ENSP00000282276.6:p.Tyr365Cys
NM_138395.3:c.1094A>G NP_612404.1:p.Tyr365Cys
NM_138395.4:c.1094A>G MANE Select NP_612404.1:p.Tyr365Cys