HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1394933T= , CM000667.2:g.1394933T= | GRCh38 |
NC_000005.9:g.1395048T= , CM000667.1:g.1395048T= | GRCh37 |
NC_000005.8:g.1448048T= | NCBI36 |
NG_015885.1:g.55496A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1840-175A= MANE Select | ENSP00000270349.9:n.1840-175A= | |
ENST00000270349.11:c.1840-175A= | ENSP00000270349.9:n.1840-175A= | |
ENST00000512002.2:n.221-175A= | ||
NM_001044.4:c.1840-175A= | NP_001035.1:n.1840-175A= | |
NM_001044.5:c.1840-175A= MANE Select | NP_001035.1:n.1840-175A= |