HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169529742A= , CM000663.2:g.169529742A= | GRCh38 |
NC_000001.10:g.169498980A= , CM000663.1:g.169498980A= | GRCh37 |
NC_000001.9:g.167765604A= | NCBI36 |
NG_011806.1:g.61790T= , LRG_553:g.61790T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367797.9:c.5285T= MANE Select | ENSP00000356771.3:p.Met1762= | |
ENST00000367796.3:c.5300T= | ENSP00000356770.3:p.Met1767= | |
ENST00000367797.7:c.5285T= | ENSP00000356771.3:p.Met1762= | |
NM_000130.4:c.5285T= , LRG_553t1:c.5285T= | NP_000121.2:p.Met1762= | |
XM_017000660.2:c.4874T= | XP_016856149.1:p.Met1625= | |
NM_000130.5:c.5285T= MANE Select | NP_000121.2:p.Met1762= |