HGVS | Genome Assembly |
---|---|
NC_000005.10:g.113387911T= , CM000667.2:g.113387911T= | GRCh38 |
NC_000005.9:g.112723608T= , CM000667.1:g.112723608T= | GRCh37 |
NC_000005.8:g.112751507T= | NCBI36 |
NG_012265.1:g.105920A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000408903.7:c.171-2699A= MANE Select | ENSP00000386227.3:n.171-2699A= | |
ENST00000408903.6:c.171-2699A= | ENSP00000386227.3:n.171-2699A= | |
NM_001085377.1:c.171-2699A= | NP_001078846.1:n.171-2699A= | |
XM_017009473.1:c.171-2699A= | XP_016864962.1:n.171-2699A= | |
NM_001085377.2:c.171-2699A= MANE Select | NP_001078846.2:n.171-2699A= |