Canonical Allele Identifier: CA350213797
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571237T>A (hg19) chr2:g.197706513T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706513T>A , CM000664.2:g.197706513T>A GRCh38
NC_000002.11:g.198571237T>A , CM000664.1:g.198571237T>A GRCh37
NC_000002.10:g.198279482T>A NCBI36
NG_034122.1:g.6210T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1108T>A MANE Select ENSP00000282276.6:p.Phe370Ile
ENST00000282276.7:c.1108T>A ENSP00000282276.6:p.Phe370Ile
NM_138395.3:c.1108T>A NP_612404.1:p.Phe370Ile
NM_138395.4:c.1108T>A MANE Select NP_612404.1:p.Phe370Ile
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