HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56005028G= , CM000674.2:g.56005028G= | GRCh38 |
NC_000012.11:g.56398812G= , CM000674.1:g.56398812G= | GRCh37 |
NC_000012.10:g.54685079G= | NCBI36 |
NG_008136.1:g.12770G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266971.8:c.*1G= MANE Select | ENSP00000266971.3:n.*1G= | |
ENST00000266971.7:c.*1G= | ENSP00000266971.3:n.*1G= | |
ENST00000356124.8:c.*1G= | ENSP00000348440.4:n.*1G= | |
ENST00000394109.7:c.*1G= | ENSP00000377668.3:n.*1G= | |
ENST00000394115.6:c.*1G= | ENSP00000377674.2:n.*1G= | |
ENST00000548274.5:c.*1G= | ENSP00000450245.1:n.*1G= | |
ENST00000550065.1:c.*1G= | ENSP00000450264.1:n.*1G= | |
NM_000456.2:c.*1G= | NP_000447.2:n.*1G= | |
NM_001032386.1:c.*1G= | NP_001027558.1:n.*1G= | |
NM_001032387.1:c.*1G= | NP_001027559.1:n.*1G= | |
XM_005269112.1:c.*1G= | XP_005269169.1:n.*1G= | |
XM_017019905.2:c.*1G= | XP_016875394.1:n.*1G= | |
XM_017019906.1:c.*1G= | XP_016875395.1:n.*1G= | |
XM_017019907.2:c.*1G= | XP_016875396.1:n.*1G= | |
XM_017019908.1:c.*1G= | XP_016875397.1:n.*1G= | |
XM_024449167.1:c.*1G= | XP_024304935.1:n.*1G= | |
NM_001032386.2:c.*1G= MANE Select | NP_001027558.1:n.*1G= | |
NM_000456.3:c.*1G= | NP_000447.2:n.*1G= | |
NM_001032387.2:c.*1G= | NP_001027559.1:n.*1G= |