HGVS | Genome Assembly |
---|---|
NC_000002.12:g.169487771T= , CM000664.2:g.169487771T= | GRCh38 |
NC_000002.11:g.170344281T= , CM000664.1:g.170344281T= | GRCh37 |
NC_000002.10:g.170052527T= | NCBI36 |
NG_011567.1:g.13276T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295240.8:c.209-35T= MANE Select | ENSP00000295240.3:n.209-35T= | |
ENST00000295240.7:c.209-35T= | ENSP00000295240.3:n.209-35T= | |
ENST00000392663.6:c.209-35T= | ENSP00000376431.2:n.209-35T= | |
ENST00000443151.1:c.143-216T= | ENSP00000406182.1:n.143-216T= | |
ENST00000475571.1:n.10T= | ||
ENST00000513963.1:c.209-35T= | ENSP00000424363.1:n.209-35T= | |
NM_152384.2:c.209-35T= | NP_689597.1:n.209-35T= | |
NM_152384.3:c.209-35T= MANE Select | NP_689597.1:n.209-35T= |