HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193122115G= , CM000663.2:g.193122115G= | GRCh38 |
NC_000001.10:g.193091245G= , CM000663.1:g.193091245G= | GRCh37 |
NC_000001.9:g.191357868G= | NCBI36 |
NG_012691.1:g.5158G= , LRG_507:g.5158G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.-86G= MANE Select | ENSP00000356405.4:n.-86G= | |
ENST00000643006.1:c.-86G= | ENSP00000496633.1:n.-86G= | |
ENST00000649895.1:n.133G= | ||
ENST00000650197.1:c.-86G= | ENSP00000496929.1:n.-86G= | |
ENST00000367435.3:c.-86G= | ENSP00000356405.3:n.-86G= | |
NM_024529.4:c.-86G= , LRG_507t1:c.-86G= | NP_078805.3:n.-86G= | |
XM_006711537.2:c.-86G= | XP_006711600.1:n.-86G= | |
XM_006711537.4:c.-86G= | XP_006711600.1:n.-86G= | |
XR_001738350.1:n.1542C= | ||
NM_024529.5:c.-86G= MANE Select | NP_078805.3:n.-86G= |