HGVS | Genome Assembly |
---|---|
NC_000006.12:g.44313360T>A , CM000668.2:g.44313360T>A | GRCh38 |
NC_000006.11:g.44281097T>A , CM000668.1:g.44281097T>A | GRCh37 |
NC_000006.10:g.44389075T>A | NCBI36 |
NG_031952.1:g.4967A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000505802.1:c.855+5718T>A | ||
NM_001318876.2:c.946-128530T>A | NP_001305805.1:n.946-128530T>A |