Canonical Allele Identifier: CA350213594
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571147C>G (hg19) chr2:g.197706423C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706423C>G , CM000664.2:g.197706423C>G GRCh38
NC_000002.11:g.198571147C>G , CM000664.1:g.198571147C>G GRCh37
NC_000002.10:g.198279392C>G NCBI36
NG_034122.1:g.6120C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1018C>G MANE Select ENSP00000282276.6:p.His340Asp
ENST00000282276.7:c.1018C>G ENSP00000282276.6:p.His340Asp
NM_138395.3:c.1018C>G NP_612404.1:p.His340Asp
NM_138395.4:c.1018C>G MANE Select NP_612404.1:p.His340Asp
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Search 100 bp 3'