HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663475T>C , CM000676.2:g.36663475T>C | GRCh38 |
NC_000014.8:g.37132680T>C , CM000676.1:g.37132680T>C | GRCh37 |
NC_000014.7:g.36202431T>C | NCBI36 |
NG_013357.1:g.10908T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361487.7:c.583T>C MANE Select | ENSP00000355245.6:p.Ser195Pro | |
ENST00000361487.6:c.583T>C | ENSP00000355245.6:p.Ser195Pro | |
ENST00000402703.6:c.583T>C | ENSP00000384817.2:p.Ser195Pro | |
ENST00000554201.1:c.22T>C | ENSP00000450434.1:p.Ser8Pro | |
NM_006194.3:c.583T>C | NP_006185.1:p.Ser195Pro | |
NM_001372076.1:c.583T>C MANE Select | NP_001359005.1:p.Ser195Pro | |
NM_006194.4:c.583T>C | NP_006185.1:p.Ser195Pro |