HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663462C= , CM000676.2:g.36663462C= | GRCh38 |
NC_000014.8:g.37132667C= , CM000676.1:g.37132667C= | GRCh37 |
NC_000014.7:g.36202418C= | NCBI36 |
NG_013357.1:g.10895C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.570C= MANE Select | ENSP00000355245.6:p.Arg190= | |
ENST00000361487.6:c.570C= | ENSP00000355245.6:p.Arg190= | |
ENST00000402703.6:c.570C= | ENSP00000384817.2:p.Arg190= | |
ENST00000554201.1:c.9C= | ENSP00000450434.1:p.Arg3= | |
NM_006194.3:c.570C= | NP_006185.1:p.Arg190= | |
NM_001372076.1:c.570C= MANE Select | NP_001359005.1:p.Arg190= | |
NM_006194.4:c.570C= | NP_006185.1:p.Arg190= |