HGVS | Genome Assembly |
---|---|
NC_000015.10:g.43599503G>A , CM000677.2:g.43599503G>A | GRCh38 |
NC_000015.9:g.43891701G>A , CM000677.1:g.43891701G>A | GRCh37 |
NC_000015.8:g.41678993G>A | NCBI36 |
NG_011636.1:g.24298C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000411560.1:n.112G>A (CKMT1B) | ||
ENST00000450892.6:c.*169C>T (STRC) | ENSP00000401513.2:n.*169C>T | |
XM_011521277.1:c.*169C>T (STRC) | XP_011519579.1:n.*169C>T | |
XM_011521278.1:c.*169C>T (STRC) | XP_011519580.1:n.*169C>T | |
XM_011521279.1:c.*169C>T (STRC) | XP_011519581.1:n.*169C>T |