Canonical Allele Identifier: CA350213567
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571135T>A (hg19) chr2:g.197706411T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706411T>A , CM000664.2:g.197706411T>A GRCh38
NC_000002.11:g.198571135T>A , CM000664.1:g.198571135T>A GRCh37
NC_000002.10:g.198279380T>A NCBI36
NG_034122.1:g.6108T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1006T>A MANE Select ENSP00000282276.6:p.Cys336Ser
ENST00000282276.7:c.1006T>A ENSP00000282276.6:p.Cys336Ser
NM_138395.3:c.1006T>A NP_612404.1:p.Cys336Ser
NM_138395.4:c.1006T>A MANE Select NP_612404.1:p.Cys336Ser
Search 100 bp 5'
Search 100 bp 3'