HGVS | Genome Assembly |
---|---|
NC_000007.14:g.74789228T= , CM000669.2:g.74789228T= | GRCh38 |
NC_000007.13:g.74203572T= , CM000669.1:g.74203572T= | GRCh37 |
NC_000007.12:g.73841508T= | NCBI36 |
NG_009078.2:g.20265T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289473.11:c.*68T= MANE Select | ENSP00000289473.4:n.*68T= | |
ENST00000289473.10:c.*68T= | ENSP00000289473.4:n.*68T= | |
ENST00000289473.8:c.*68T= | ENSP00000289473.4:n.*68T= | |
ENST00000398421.6:n.2268T= | ||
ENST00000455062.2:n.1350T= | ||
NM_000265.5:c.*68T= | NP_000256.4:n.*68T= | |
XM_005250543.3:c.*162T= | XP_005250600.2:n.*162T= | |
XM_011516498.1:c.*115T= | XP_011514800.1:n.*115T= | |
XM_011516501.1:c.*68T= | XP_011514803.1:n.*68T= | |
NM_000265.6:c.*68T= | NP_000256.4:n.*68T= | |
NM_000265.7:c.*68T= MANE Select | NP_000256.4:n.*68T= |