Canonical Allele Identifier: CA430823703
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571146C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706422C>G , CM000664.2:g.197706422C>G GRCh38
NC_000002.11:g.198571146C>G , CM000664.1:g.198571146C>G GRCh37
NC_000002.10:g.198279391C>G NCBI36
NG_034122.1:g.6119C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282276.8:c.1017C>G MANE Select ENSP00000282276.6:p.Ser339=
ENST00000282276.7:c.1017C>G ENSP00000282276.6:p.Ser339=
NM_138395.3:c.1017C>G NP_612404.1:p.Ser339=
NM_138395.4:c.1017C>G MANE Select NP_612404.1:p.Ser339=