HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186194129T>C , CM000666.2:g.186194129T>C | GRCh38 |
NC_000004.11:g.187115283T>C , CM000666.1:g.187115283T>C | GRCh37 |
NC_000004.10:g.187352277T>C | NCBI36 |
NG_007965.1:g.7610T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.215-371T>C MANE Select | ENSP00000368079.4:n.215-371T>C | |
ENST00000378802.4:c.215-371T>C | ENSP00000368079.4:n.215-371T>C | |
NM_207352.3:c.215-371T>C | NP_997235.3:n.215-371T>C | |
XM_005262935.2:c.215-371T>C | XP_005262992.1:n.215-371T>C | |
XM_005262935.4:c.215-371T>C | XP_005262992.1:n.215-371T>C | |
XM_017008037.1:c.-96-371T>C | XP_016863526.1:n.-96-371T>C | |
NM_207352.4:c.215-371T>C MANE Select | NP_997235.3:n.215-371T>C |