HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186191708G= , CM000666.2:g.186191708G= | GRCh38 |
NC_000004.11:g.187112862G= , CM000666.1:g.187112862G= | GRCh37 |
NC_000004.10:g.187349856G= | NCBI36 |
NG_007965.1:g.5189G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.-116G= MANE Select | ENSP00000368079.4:n.-116G= | |
ENST00000378802.4:c.-116G= | ENSP00000368079.4:n.-116G= | |
NM_207352.3:c.-116G= | NP_997235.3:n.-116G= | |
XM_005262935.2:c.-116G= | XP_005262992.1:n.-116G= | |
XM_017008037.1:c.-426G= | XP_016863526.1:n.-426G= | |
NM_207352.4:c.-116G= MANE Select | NP_997235.3:n.-116G= |