HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193122120G= , CM000663.2:g.193122120G= | GRCh38 |
NC_000001.10:g.193091250G= , CM000663.1:g.193091250G= | GRCh37 |
NC_000001.9:g.191357873G= | NCBI36 |
NG_012691.1:g.5163G= , LRG_507:g.5163G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.-81G= MANE Select | ENSP00000356405.4:n.-81G= | |
ENST00000643006.1:c.-81G= | ENSP00000496633.1:n.-81G= | |
ENST00000649895.1:n.138G= | ||
ENST00000650197.1:c.-81G= | ENSP00000496929.1:n.-81G= | |
ENST00000367435.3:c.-81G= | ENSP00000356405.3:n.-81G= | |
NM_024529.4:c.-81G= , LRG_507t1:c.-81G= | NP_078805.3:n.-81G= | |
XM_006711537.2:c.-81G= | XP_006711600.1:n.-81G= | |
XM_006711537.4:c.-81G= | XP_006711600.1:n.-81G= | |
XR_001738350.1:n.1537C= | ||
NM_024529.5:c.-81G= MANE Select | NP_078805.3:n.-81G= |