HGVS | Genome Assembly |
---|---|
NC_000007.14:g.74789186G= , CM000669.2:g.74789186G= | GRCh38 |
NC_000007.13:g.74203530G= , CM000669.1:g.74203530G= | GRCh37 |
NC_000007.12:g.73841466G= | NCBI36 |
NG_009078.2:g.20223G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000289473.11:c.*26G= MANE Select | ENSP00000289473.4:n.*26G= | |
ENST00000289473.10:c.*26G= | ENSP00000289473.4:n.*26G= | |
ENST00000289473.8:c.*26G= | ENSP00000289473.4:n.*26G= | |
ENST00000398421.6:n.2226G= | ||
ENST00000455062.2:n.1308G= | ||
NM_000265.5:c.*26G= | NP_000256.4:n.*26G= | |
XM_005250543.3:c.*120G= | XP_005250600.2:n.*120G= | |
XM_011516498.1:c.*73G= | XP_011514800.1:n.*73G= | |
XM_011516501.1:c.*26G= | XP_011514803.1:n.*26G= | |
NM_000265.6:c.*26G= | NP_000256.4:n.*26G= | |
NM_000265.7:c.*26G= MANE Select | NP_000256.4:n.*26G= |