HGVS | Genome Assembly |
---|---|
NC_000012.12:g.102917250A= , CM000674.2:g.102917250A= | GRCh38 |
NC_000012.11:g.103311028A= , CM000674.1:g.103311028A= | GRCh37 |
NC_000012.10:g.101835158A= | NCBI36 |
NG_008690.1:g.5353T= | |
NG_008690.2:g.46161T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307000.7:c.-267T= | ENSP00000303500.2:n.-267T= | |
ENST00000546708.5:n.493-25T= | ||
ENST00000546844.1:c.-95-25T= | ENSP00000446658.1:n.-95-25T= | |
ENST00000547319.1:n.217-25T= | ||
ENST00000551337.5:c.-95-25T= | ENSP00000447620.1:n.-95-25T= | |
ENST00000553106.5:c.-120T= | ENSP00000448059.1:n.-120T= | |
ENST00000635500.1:n.29-4352T= | ||
NM_000277.1:c.-120T= | NP_000268.1:n.-120T= | |
NM_000277.2:c.-120T= | NP_000268.1:n.-120T= | |
NM_001354304.1:c.-95-25T= | NP_001341233.1:n.-95-25T= | |
NM_001354304.2:c.-95-25T= | NP_001341233.1:n.-95-25T= |