HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218749T= , CM000676.2:g.93218749T= | GRCh38 |
NC_000014.8:g.93685095T= , CM000676.1:g.93685095T= | GRCh37 |
NC_000014.7:g.92754848T= | NCBI36 |
NG_051089.1:g.16694T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000013070.11:c.810+14T= MANE Select | ENSP00000013070.6:n.810+14T= | |
ENST00000013070.10:c.810+14T= | ENSP00000013070.6:n.810+14T= | |
ENST00000416753.5:c.582+14T= | ENSP00000391706.2:n.582+14T= | |
ENST00000553674.1:c.*511+14T= | ENSP00000450470.1:n.*511+14T= | |
ENST00000553857.5:c.378+3468T= | ||
ENST00000555329.1:c.55+14T= | ||
NM_175748.3:c.810+14T= | NP_786924.2:n.810+14T= | |
NR_038150.1:n.912+14T= | ||
NM_175748.4:c.810+14T= MANE Select | NP_786924.2:n.810+14T= | |
NR_038150.2:n.712+14T= |