HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44118616G>C , CM000682.2:g.44118616G>C | GRCh38 |
NC_000020.10:g.42747256G>C , CM000682.1:g.42747256G>C | GRCh37 |
NC_000020.9:g.42180670G>C | NCBI36 |
NG_031867.1:g.73963C>G , LRG_394:g.73963C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372980.4:c.1177C>G MANE Select | ENSP00000362071.3:p.His393Asp | |
ENST00000372980.3:c.1177C>G | ENSP00000362071.3:p.His393Asp | |
NM_020433.4:c.1177C>G , LRG_394t1:c.1177C>G | NP_065166.2:p.His393Asp | |
XM_006723832.2:c.1177C>G | XP_006723895.1:p.His393Asp | |
NM_020433.5:c.1177C>G MANE Select | NP_065166.2:p.His393Asp |