Canonical Allele Identifier: CA350213769
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571226C>A (hg19) chr2:g.197706502C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706502C>A , CM000664.2:g.197706502C>A GRCh38
NC_000002.11:g.198571226C>A , CM000664.1:g.198571226C>A GRCh37
NC_000002.10:g.198279471C>A NCBI36
NG_034122.1:g.6199C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1097C>A MANE Select ENSP00000282276.6:p.Thr366Asn
ENST00000282276.7:c.1097C>A ENSP00000282276.6:p.Thr366Asn
NM_138395.3:c.1097C>A NP_612404.1:p.Thr366Asn
NM_138395.4:c.1097C>A MANE Select NP_612404.1:p.Thr366Asn
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