HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46118271A= , CM000682.2:g.46118271A= | GRCh38 |
NC_000020.10:g.44746910A= , CM000682.1:g.44746910A= | GRCh37 |
NC_000020.9:g.44180317A= | NCBI36 |
NG_007279.1:g.5005A= , LRG_40:g.5005A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695669.1:n.1A= | ||
NM_001250.5:c.-73A= | NP_001241.1:n.-73A= | |
NM_001302753.1:c.-73A= | NP_001289682.1:n.-73A= | |
NM_152854.3:c.-73A= | NP_690593.1:n.-73A= | |
NR_126502.1:n.18A= | ||
XM_005260617.2:c.-73A= | XP_005260674.1:n.-73A= | |
XM_005260619.2:c.-73A= | XP_005260676.1:n.-73A= | |
XM_011529109.1:c.-73A= | XP_011527411.1:n.-73A= | |
XR_936660.1:n.22A= | ||
NM_001322421.1:c.-73A= | NP_001309350.1:n.-73A= | |
NM_001322422.1:c.-73A= | NP_001309351.1:n.-73A= | |
NM_001362758.1:c.-73A= | NP_001349687.1:n.-73A= | |
NR_136327.1:n.18A= | ||
XM_005260619.3:c.-73A= | XP_005260676.1:n.-73A= | |
XM_011529109.2:c.-73A= | XP_011527411.1:n.-73A= | |
XM_017028135.1:c.-73A= | XP_016883624.1:n.-73A= | |
XM_017028136.1:c.-73A= | XP_016883625.1:n.-73A= |