HGVS | Genome Assembly |
---|---|
NC_000017.11:g.35880429A= , CM000679.2:g.35880429A= | GRCh38 |
NC_000017.9:g.31231546A= | NCBI36 |
NG_015990.1:g.4945T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000603197.6:c.-124T= | ENSP00000474412.1:n.-124T= | |
ENST00000605509.2:c.-17-107T= | ENSP00000474141.2:n.-17-107T= | |
ENST00000603197.5:c.-124T= | ENSP00000474412.1:n.-124T= | |
ENST00000605140.5:c.-17-107T= | ENSP00000475057.1:n.-17-107T= | |
XR_934696.1:n.197-3953A= | ||
XR_934697.1:n.200-3953A= | ||
XR_001752852.1:n.426+355A= | ||
XR_934696.2:n.91-3953A= | ||
XR_934697.2:n.91-3953A= |