HGVS | Genome Assembly |
---|---|
NC_000015.10:g.38351669G= , CM000677.2:g.38351669G= | GRCh38 |
NC_000015.9:g.38643870G= , CM000677.1:g.38643870G= | GRCh37 |
NC_000015.8:g.36431162G= | NCBI36 |
NG_008980.1:g.103819G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299084.9:c.*5G= MANE Select | ENSP00000299084.4:n.*5G= | |
ENST00000299084.8:c.*5G= | ENSP00000299084.4:n.*5G= | |
NM_152594.2:c.*5G= | NP_689807.1:n.*5G= | |
XM_005254202.2:c.*5G= | XP_005254259.1:n.*5G= | |
XM_005254203.3:c.*5G= | XP_005254260.1:n.*5G= | |
XM_011521288.1:c.*5G= | XP_011519590.1:n.*5G= | |
XM_011521289.1:c.*5G= | XP_011519591.1:n.*5G= | |
XM_011521290.1:c.*5G= | XP_011519592.1:n.*5G= | |
XM_005254202.3:c.*5G= | XP_005254259.1:n.*5G= | |
XM_011521289.3:c.*5G= | XP_011519591.1:n.*5G= | |
NM_152594.3:c.*5G= MANE Select | NP_689807.1:n.*5G= |