Canonical Allele Identifier: CA350213589
Gene: MARS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.198571144T>C (hg19) chr2:g.197706420T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706420T>C , CM000664.2:g.197706420T>C GRCh38
NC_000002.11:g.198571144T>C , CM000664.1:g.198571144T>C GRCh37
NC_000002.10:g.198279389T>C NCBI36
NG_034122.1:g.6117T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.1015T>C MANE Select ENSP00000282276.6:p.Ser339Pro
ENST00000282276.7:c.1015T>C ENSP00000282276.6:p.Ser339Pro
NM_138395.3:c.1015T>C NP_612404.1:p.Ser339Pro
NM_138395.4:c.1015T>C MANE Select NP_612404.1:p.Ser339Pro
Search 100 bp 5'
Search 100 bp 3'