HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120739400C>A , CM000674.2:g.120739400C>A | GRCh38 |
NC_000012.11:g.121177203C>A , CM000674.1:g.121177203C>A | GRCh37 |
NC_000012.10:g.119661586C>A | NCBI36 |
NG_007991.1:g.18633C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242592.9:c.1191C>A MANE Select | ENSP00000242592.4:p.Ile397= | |
ENST00000242592.8:c.1191C>A | ENSP00000242592.4:p.Ile397= | |
ENST00000411593.2:c.1179C>A | ENSP00000401045.2:p.Ile393= | |
NM_000017.3:c.1191C>A | NP_000008.1:p.Ile397= | |
NM_001302554.1:c.1179C>A | NP_001289483.1:p.Ile393= | |
NM_000017.4:c.1191C>A MANE Select | NP_000008.1:p.Ile397= | |
NM_001302554.2:c.1179C>A | NP_001289483.1:p.Ile393= |