HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57765079C= , CM000674.2:g.57765079C= | GRCh38 |
NC_000012.11:g.58158862C= , CM000674.1:g.58158862C= | GRCh37 |
NC_000012.10:g.56445129C= | NCBI36 |
NG_007076.1:g.7115G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000546609.2:n.634G= | ||
ENST00000713544.1:c.803G= | ENSP00000518840.1:p.Trp268= | |
ENST00000713545.1:c.780G= | ENSP00000518841.1:p.Leu260= | |
ENST00000228606.9:c.722G= MANE Select | ENSP00000228606.4:p.Trp241= | |
ENST00000228606.8:c.722G= | ENSP00000228606.4:p.Trp241= | |
ENST00000546567.5:c.17G= | ENSP00000449472.1:p.Trp6= | |
ENST00000546609.1:c.634G= | ||
ENST00000547344.5:n.861G= | ||
ENST00000547451.1:n.522G= | ||
NM_000785.3:c.722G= | NP_000776.1:p.Trp241= | |
NM_000785.4:c.722G= MANE Select | NP_000776.1:p.Trp241= |