HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71943096T= , CM000674.2:g.71943096T= | GRCh38 |
NC_000012.11:g.72336876T= , CM000674.1:g.72336876T= | GRCh37 |
NC_000012.10:g.70623143T= | NCBI36 |
NG_008279.1:g.9251T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333850.4:c.256-1198T= MANE Select | ENSP00000329093.3:n.256-1198T= | |
ENST00000333850.3:c.256-1198T= | ENSP00000329093.3:n.256-1198T= | |
ENST00000546576.1:n.266-1198T= | ||
NM_173353.3:c.256-1198T= | NP_775489.2:n.256-1198T= | |
XR_245894.2:n.356-1198T= | ||
XR_001748575.1:n.356-1198T= | ||
NM_173353.4:c.256-1198T= MANE Select | NP_775489.2:n.256-1198T= |