HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312928T= , CM000673.2:g.118312928T= | GRCh38 |
NC_000011.9:g.118183643T= , CM000673.1:g.118183643T= | GRCh37 |
NC_000011.8:g.117688853T= | NCBI36 |
NG_007383.1:g.13349T= , LRG_38:g.13349T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.352+62T= MANE Select | ENSP00000354566.4:n.352+62T= | |
ENST00000361763.8:c.352+62T= | ENSP00000354566.4:n.352+62T= | |
ENST00000526146.5:n.960T= | ||
ENST00000528435.5:n.905+62T= | ||
ENST00000528600.1:c.334+62T= | ENSP00000433975.1:n.334+62T= | |
ENST00000529713.5:n.520T= | ||
ENST00000531913.1:n.723+62T= | ||
NM_000733.3:c.352+62T= , LRG_38t1:c.352+62T= | NP_000724.1:n.352+62T= | |
NM_000733.4:c.352+62T= MANE Select | NP_000724.1:n.352+62T= |