HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4898645G= , CM000679.2:g.4898645G= | GRCh38 |
NC_000017.10:g.4801940G= , CM000679.1:g.4801940G= | GRCh37 |
NC_000017.9:g.4742719G= | NCBI36 |
NG_008029.2:g.9431C= | |
NG_028005.1:g.70306G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649488.2:c.*91C= MANE Select | ENSP00000497829.1:n.*91C= | |
ENST00000649830.1:c.*209C= | ENSP00000496907.1:n.*209C= | |
ENST00000652550.1:n.1299C= | ||
ENST00000293780.4:c.*91C= | ENSP00000293780.4:n.*91C= | |
ENST00000572438.1:n.1259C= | ||
NM_000080.3:c.*91C= | NP_000071.1:n.*91C= | |
NM_000080.4:c.*91C= MANE Select | NP_000071.1:n.*91C= | |
XM_017024115.1:c.*91C= | XP_016879604.1:n.*91C= |