HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68429981A>G , CM000663.2:g.68429981A>G | GRCh38 |
NC_000001.10:g.68895664A>G , CM000663.1:g.68895664A>G | GRCh37 |
NC_000001.9:g.68668252A>G | NCBI36 |
NG_008472.1:g.24979T>C | |
NG_008472.2:g.24979T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1451-54T>C MANE Select | ENSP00000262340.5:n.1451-54T>C | |
ENST00000262340.5:c.1451-54T>C | ENSP00000262340.5:n.1451-54T>C | |
NM_000329.2:c.1451-54T>C | NP_000320.1:n.1451-54T>C | |
XM_017002027.1:c.1175-54T>C | XP_016857516.1:n.1175-54T>C | |
NM_000329.3:c.1451-54T>C MANE Select | NP_000320.1:n.1451-54T>C |