Canonical Allele Identifier: CA350213592
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571145C>T (hg19) chr2:g.197706421C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706421C>T , CM000664.2:g.197706421C>T GRCh38
NC_000002.11:g.198571145C>T , CM000664.1:g.198571145C>T GRCh37
NC_000002.10:g.198279390C>T NCBI36
NG_034122.1:g.6118C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282276.8:c.1016C>T MANE Select ENSP00000282276.6:p.Ser339Phe
ENST00000282276.7:c.1016C>T ENSP00000282276.6:p.Ser339Phe
NM_138395.3:c.1016C>T NP_612404.1:p.Ser339Phe
NM_138395.4:c.1016C>T MANE Select NP_612404.1:p.Ser339Phe
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