HGVS | Genome Assembly |
---|---|
NC_000012.12:g.101830819G= , CM000674.2:g.101830819G= | GRCh38 |
NC_000012.11:g.102224597G= , CM000674.1:g.102224597G= | GRCh37 |
NC_000012.10:g.100748728G= | NCBI36 |
NG_021243.1:g.5049C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299314.12:c.-144C= MANE Select | ENSP00000299314.7:n.-144C= | |
ENST00000299314.11:c.-144C= | ENSP00000299314.7:n.-144C= | |
ENST00000392919.4:c.-144C= | ENSP00000376651.4:n.-144C= | |
NM_024312.4:c.-144C= | NP_077288.2:n.-144C= | |
XM_006719593.2:c.-144C= | XP_006719656.1:n.-144C= | |
XM_017019961.1:c.-293C= | XP_016875450.1:n.-293C= | |
NM_024312.5:c.-144C= MANE Select | NP_077288.2:n.-144C= |