HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12904640T= , CM000686.2:g.12904640T= | GRCh38 |
NC_000024.9:g.15016551T= , CM000686.1:g.15016551T= | GRCh37 |
NC_000024.8:g.13525945T= | NCBI36 |
NG_012831.1:g.5533T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360160.8:c.-3+226T= | ENSP00000353284.4:n.-3+226T= | |
ENST00000454054.5:c.-79-218T= | ENSP00000398953.1:n.-79-218T= | |
NM_001122665.2:c.-3+226T= | NP_001116137.1:n.-3+226T= | |
NM_001122665.3:c.-3+226T= | NP_001116137.1:n.-3+226T= |