HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022634T= , CM000663.2:g.17022634T= | GRCh38 |
NC_000001.10:g.17349129T= , CM000663.1:g.17349129T= | GRCh37 |
NC_000001.9:g.17221716T= | NCBI36 |
NG_012340.1:g.36537A= , LRG_316:g.36537A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.568A= | ENSP00000481376.2:p.Met190= | |
ENST00000491274.6:c.697A= | ENSP00000480482.2:p.Met233= | |
ENST00000375499.8:c.739A= MANE Select | ENSP00000364649.3:p.Met247= | |
ENST00000375499.7:c.739A= | ENSP00000364649.3:p.Met247= | |
ENST00000475049.5:n.164A= | ||
ENST00000485092.5:n.403A= | ||
ENST00000485515.5:n.673A= | ||
NM_003000.2:c.739A= , LRG_316t1:c.739A= | NP_002991.2:p.Met247= | |
NM_003000.3:c.739A= MANE Select | NP_002991.2:p.Met247= |