HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459247A= , CM000668.2:g.49459247A= | GRCh38 |
NC_000006.11:g.49426960A= , CM000668.1:g.49426960A= | GRCh37 |
NC_000006.10:g.49534919A= | NCBI36 |
NG_007100.1:g.8893T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.220T= MANE Select | ENSP00000274813.3:p.Ser74= | |
ENST00000274813.3:c.220T= | ENSP00000274813.3:p.Ser74= | |
NM_000255.3:c.220T= | NP_000246.2:p.Ser74= | |
XM_005249143.2:c.220T= | XP_005249200.1:p.Ser74= | |
XM_005249143.3:c.220T= | XP_005249200.1:p.Ser74= | |
NM_000255.4:c.220T= MANE Select | NP_000246.2:p.Ser74= |