HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736145A>C , CM000685.2:g.153736145A>C | GRCh38 |
NC_000023.10:g.153001599A>C , CM000685.1:g.153001599A>C | GRCh37 |
NC_000023.9:g.152654793A>C | NCBI36 |
NG_009022.2:g.16278A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1115A>C MANE Select | ENSP00000218104.3:p.Lys372Thr | |
ENST00000218104.5:c.1115A>C | ENSP00000218104.3:p.Lys372Thr | |
ENST00000443684.2:n.118A>C | ||
NM_000033.3:c.1115A>C | NP_000024.2:p.Lys372Thr | |
XR_938507.1:n.1531A>C | ||
XR_938507.2:n.1531A>C | ||
NM_000033.4:c.1115A>C MANE Select | NP_000024.2:p.Lys372Thr |