HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1423659C= , CM000667.2:g.1423659C= | GRCh38 |
NC_000005.9:g.1423774C= , CM000667.1:g.1423774C= | GRCh37 |
NC_000005.8:g.1476774C= | NCBI36 |
NG_015885.1:g.26770G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.654-1645G= MANE Select | ENSP00000270349.9:n.654-1645G= | |
ENST00000270349.11:c.654-1645G= | ENSP00000270349.9:n.654-1645G= | |
NM_001044.4:c.654-1645G= | NP_001035.1:n.654-1645G= | |
NM_001044.5:c.654-1645G= MANE Select | NP_001035.1:n.654-1645G= |