HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10175864A>T , CM000668.2:g.10175864A>T | GRCh38 |
NC_000006.11:g.10176097A>T , CM000668.1:g.10176097A>T | GRCh37 |
NC_000006.10:g.10284083A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000462111.1:n.164-16365T>A | ||
ENST00000481704.1:c.-101-16365T>A | ENSP00000418286.1:n.-101-16365T>A | |
XM_017011612.1:c.-101-16365T>A | XP_016867101.1:n.-101-16365T>A | |
NR_170155.1:n.232-16365T>A |