HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94401325G= , CM000669.2:g.94401325G= | GRCh38 |
NC_000007.13:g.94030637G= , CM000669.1:g.94030637G= | GRCh37 |
NC_000007.12:g.93868573G= | NCBI36 |
NG_007405.1:g.11765G= , LRG_2:g.11765G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.226-242G= MANE Select | ENSP00000297268.6:n.226-242G= | |
ENST00000297268.10:c.226-242G= | ENSP00000297268.6:n.226-242G= | |
ENST00000620463.1:c.220-242G= | ENSP00000477719.1:n.220-242G= | |
NM_000089.3:c.226-242G= , LRG_2t1:c.226-242G= | NP_000080.2:n.226-242G= | |
NM_000089.4:c.226-242G= MANE Select | NP_000080.2:n.226-242G= |