HGVS | Genome Assembly |
---|---|
NC_000012.12:g.102917313A= , CM000674.2:g.102917313A= | GRCh38 |
NC_000012.11:g.103311091A= , CM000674.1:g.103311091A= | GRCh37 |
NC_000012.10:g.101835221A= | NCBI36 |
NG_008690.1:g.5291T= | |
NG_008690.2:g.46098T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546708.5:n.493-88T= | ||
ENST00000546844.1:c.-95-88T= | ENSP00000446658.1:n.-95-88T= | |
ENST00000547319.1:n.217-88T= | ||
ENST00000551337.5:c.-95-88T= | ENSP00000447620.1:n.-95-88T= | |
ENST00000553106.5:c.-183T= | ENSP00000448059.1:n.-183T= | |
ENST00000635500.1:n.29-4415T= | ||
NM_000277.1:c.-182T= | NP_000268.1:n.-182T= | |
NM_000277.2:c.-183T= | NP_000268.1:n.-183T= | |
NM_001354304.1:c.-95-88T= | NP_001341233.1:n.-95-88T= | |
NM_001354304.2:c.-95-88T= | NP_001341233.1:n.-95-88T= |