HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20618469C= , CM000663.2:g.20618469C= | GRCh38 |
NC_000001.10:g.20944962C= , CM000663.1:g.20944962C= | GRCh37 |
NC_000001.9:g.20817549C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375071.4:c.342C= MANE Select | ENSP00000364212.3:p.Pro114= | |
ENST00000375071.3:c.342C= | ENSP00000364212.3:p.Pro114= | |
ENST00000461985.1:n.328C= | ||
NM_001785.2:c.342C= | NP_001776.1:p.Pro114= | |
NM_001785.3:c.342C= MANE Select | NP_001776.1:p.Pro114= |