HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154371254G= , CM000685.2:g.154371254G= | GRCh38 |
NC_000023.10:g.153599622G= , CM000685.1:g.153599622G= | GRCh37 |
NC_000023.9:g.153252816G= | NCBI36 |
NG_008677.1:g.1827G= , LRG_745:g.1827G= | |
NG_011506.1:g.8385C= | |
NG_011506.2:g.8385C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360319.9:c.-9C= | ENSP00000353467.4:n.-9C= | |
ENST00000369850.10:c.-9C= MANE Select | ENSP00000358866.3:n.-9C= | |
ENST00000422373.6:c.-9C= | ENSP00000416926.2:n.-9C= | |
ENST00000344736.8:c.-9C= | ENSP00000358863.3:n.-9C= | |
ENST00000360319.8:c.-9C= | ENSP00000353467.4:n.-9C= | |
ENST00000369850.7:c.-9C= | ENSP00000358866.3:n.-9C= | |
ENST00000422373.5:c.-9C= | ENSP00000416926.1:n.-9C= | |
ENST00000610817.4:c.-90C= | ENSP00000480593.1:n.-90C= | |
NM_001110556.1:c.-9C= | NP_001104026.1:n.-9C= | |
NM_001456.3:c.-9C= | NP_001447.2:n.-9C= | |
XM_011531127.1:c.-9C= | XP_011529429.1:n.-9C= | |
XM_011531128.1:c.-9C= | XP_011529430.1:n.-9C= | |
XM_011531129.1:c.-9C= | XP_011529431.1:n.-9C= | |
XM_011531130.1:c.-9C= | XP_011529432.1:n.-9C= | |
XM_011531131.1:c.-9C= | XP_011529433.1:n.-9C= | |
NM_001110556.2:c.-9C= MANE Select | NP_001104026.1:n.-9C= | |
NM_001456.4:c.-9C= | NP_001447.2:n.-9C= |