Canonical Allele Identifier: CA1319360365
Gene: MARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706409T= , CM000664.2:g.197706409T= GRCh38
NC_000002.11:g.198571133T= , CM000664.1:g.198571133T= GRCh37
NC_000002.10:g.198279378T= NCBI36
NG_034122.1:g.6106T=

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1004T= MANE Select ENSP00000282276.6:p.Ile335=
ENST00000282276.7:c.1004T= ENSP00000282276.6:p.Ile335=
NM_138395.3:c.1004T= NP_612404.1:p.Ile335=
NM_138395.4:c.1004T= MANE Select NP_612404.1:p.Ile335=