Canonical Allele Identifier: CA62878812
Gene: MARS2 HGNC NCBI

Linked Data

dbSNP Id: rs907858752

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197706402C>T , CM000664.2:g.197706402C>T GRCh38
NC_000002.11:g.198571126C>T , CM000664.1:g.198571126C>T GRCh37
NC_000002.10:g.198279371C>T NCBI36
NG_034122.1:g.6099C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282276.8:c.997C>T MANE Select ENSP00000282276.6:p.Gln333Ter
ENST00000282276.7:c.997C>T ENSP00000282276.6:p.Gln333Ter
NM_138395.3:c.997C>T NP_612404.1:p.Gln333Ter
NM_138395.4:c.997C>T MANE Select NP_612404.1:p.Gln333Ter