HGVS | Genome Assembly |
---|---|
NC_000011.10:g.113475629T>A , CM000673.2:g.113475629T>A | GRCh38 |
NC_000011.9:g.113346351T>A , CM000673.1:g.113346351T>A | GRCh37 |
NC_000011.8:g.112851561T>A | NCBI36 |
NG_008841.1:g.4651A>T |
HGVS | Amino-acid Change |
---|---|
ENST00000540600.5:n.34+29A>T | |
XR_948024.2:n.813A>T |