HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21854376T= , CM000669.2:g.21854376T= | GRCh38 |
NC_000007.13:g.21893994T= , CM000669.1:g.21893994T= | GRCh37 |
NC_000007.12:g.21860519T= | NCBI36 |
NG_012886.2:g.316162T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000409508.8:c.11123T= MANE Select | ENSP00000475939.1:p.Val3708= | |
ENST00000328843.10:c.11144T= | ENSP00000330671.7:p.Val3715= | |
ENST00000409508.7:c.11123T= | ENSP00000475939.1:p.Val3708= | |
ENST00000421290.1:n.306T= | ||
ENST00000607413.5:n.386T= | ||
ENST00000620169.4:c.11144T= | ENSP00000481693.1:p.Val3715= | |
NM_001277115.1:c.11123T= | NP_001264044.1:p.Val3708= | |
NM_001277115.2:c.11123T= MANE Select | NP_001264044.1:p.Val3708= |