HGVS | Genome Assembly |
---|---|
NC_000007.14:g.74789217T= , CM000669.2:g.74789217T= | GRCh38 |
NC_000007.13:g.74203561T= , CM000669.1:g.74203561T= | GRCh37 |
NC_000007.12:g.73841497T= | NCBI36 |
NG_009078.2:g.20254T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289473.11:c.*57T= MANE Select | ENSP00000289473.4:n.*57T= | |
ENST00000289473.10:c.*57T= | ENSP00000289473.4:n.*57T= | |
ENST00000289473.8:c.*57T= | ENSP00000289473.4:n.*57T= | |
ENST00000398421.6:n.2257T= | ||
ENST00000455062.2:n.1339T= | ||
NM_000265.5:c.*57T= | NP_000256.4:n.*57T= | |
XM_005250543.3:c.*151T= | XP_005250600.2:n.*151T= | |
XM_011516498.1:c.*104T= | XP_011514800.1:n.*104T= | |
XM_011516501.1:c.*57T= | XP_011514803.1:n.*57T= | |
NM_000265.6:c.*57T= | NP_000256.4:n.*57T= | |
NM_000265.7:c.*57T= MANE Select | NP_000256.4:n.*57T= |