HGVS | Genome Assembly |
---|---|
NC_000003.12:g.8733389T>A , CM000665.2:g.8733389T>A | GRCh38 |
NC_000003.11:g.8775075T>A , CM000665.1:g.8775075T>A | GRCh37 |
NC_000003.10:g.8750075T>A | NCBI36 |
NG_008797.2:g.4580T>A , LRG_329:g.4580T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435138.5:c.64+9070A>T | ENSP00000412333.1:n.64+9070A>T | |
ENST00000478513.1:n.335+9070A>T | ||
XR_940435.1:n.330+9070A>T | ||
XM_017006530.1:c.-283+9070A>T | XP_016862019.1:n.-283+9070A>T |