HGVS | Genome Assembly |
---|---|
NC_000016.10:g.81315284G= , CM000678.2:g.81315284G= | GRCh38 |
NC_000016.9:g.81348889G= , CM000678.1:g.81348889G= | GRCh37 |
NC_000016.8:g.79906390G= | NCBI36 |
NG_009007.1:g.5319G= , LRG_242:g.5319G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648349.2:c.167+4G= | ENSP00000498114.1:n.167+4G= | |
ENST00000648994.2:c.167+4G= MANE Select | ENSP00000497351.1:n.167+4G= | |
ENST00000650388.1:c.167+4G= | ENSP00000498081.1:n.167+4G= | |
ENST00000674788.1:n.292+4G= | ||
ENST00000568107.2:c.167+4G= | ENSP00000476795.1:n.167+4G= | |
NM_022041.3:c.167+4G= , LRG_242t1:c.167+4G= | NP_071324.1:n.167+4G= | |
XM_017023734.1:c.-358+4G= | XP_016879223.1:n.-358+4G= | |
NM_001377486.1:c.-358+4G= | NP_001364415.1:n.-358+4G= | |
NM_022041.4:c.167+4G= MANE Select | NP_071324.1:n.167+4G= |