Canonical Allele Identifier: CA350213799
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571238T>A (hg19) chr2:g.197706514T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706514T>A , CM000664.2:g.197706514T>A GRCh38
NC_000002.11:g.198571238T>A , CM000664.1:g.198571238T>A GRCh37
NC_000002.10:g.198279483T>A NCBI36
NG_034122.1:g.6211T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282276.8:c.1109T>A MANE Select ENSP00000282276.6:p.Phe370Tyr
ENST00000282276.7:c.1109T>A ENSP00000282276.6:p.Phe370Tyr
NM_138395.3:c.1109T>A NP_612404.1:p.Phe370Tyr
NM_138395.4:c.1109T>A MANE Select NP_612404.1:p.Phe370Tyr
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