HGVS | Genome Assembly |
---|---|
NC_000001.11:g.67009264A= , CM000663.2:g.67009264A= | GRCh38 |
NC_000001.10:g.67474947A= , CM000663.1:g.67474947A= | GRCh37 |
NC_000001.9:g.67247535A= | NCBI36 |
NG_012933.1:g.50134T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000235345.6:c.877-97T= MANE Select | ENSP00000235345.5:n.877-97T= | |
ENST00000235345.5:c.877-97T= | ENSP00000235345.5:n.877-97T= | |
NM_015139.2:c.877-97T= | NP_055954.1:n.877-97T= | |
XM_006710478.1:c.958-97T= | XP_006710541.1:n.958-97T= | |
XM_011541070.1:c.958-97T= | XP_011539372.1:n.958-97T= | |
XM_006710478.2:c.958-97T= | XP_006710541.1:n.958-97T= | |
XM_011541070.2:c.958-97T= | XP_011539372.1:n.958-97T= | |
XR_001737057.2:n.1461-97T= | ||
XR_001737058.2:n.2246-97T= | ||
NM_015139.3:c.877-97T= MANE Select | NP_055954.1:n.877-97T= |