HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10175648T= , CM000668.2:g.10175648T= | GRCh38 |
NC_000006.11:g.10175881T= , CM000668.1:g.10175881T= | GRCh37 |
NC_000006.10:g.10283867T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000462111.1:n.164-16149A= | ||
ENST00000481704.1:c.-101-16149A= | ENSP00000418286.1:n.-101-16149A= | |
XM_017011612.1:c.-101-16149A= | XP_016867101.1:n.-101-16149A= | |
NR_170155.1:n.232-16149A= |