HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443631T= , CM000668.2:g.32443631T= | GRCh38 |
NC_000006.11:g.32411408T= , CM000668.1:g.32411408T= | GRCh37 |
NC_000006.10:g.32519386T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.611-125T= MANE Select | ENSP00000378786.2:n.611-125T= | |
ENST00000374982.5:c.536-125T= | ENSP00000364121.5:n.536-125T= | |
ENST00000395388.6:c.611-125T= | ENSP00000378786.2:n.611-125T= | |
NM_019111.4:c.611-125T= | NP_061984.2:n.611-125T= | |
NM_019111.5:c.611-125T= MANE Select | NP_061984.2:n.611-125T= |