HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135817403C= , CM000664.2:g.135817403C= | GRCh38 |
NC_000002.11:g.136574973C= , CM000664.1:g.136574973C= | GRCh37 |
NC_000002.10:g.136291443C= | NCBI36 |
NG_008104.2:g.42767G= , LRG_338:g.42767G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.1645G= MANE Select | ENSP00000264162.2:p.Ala549= | |
ENST00000264162.6:c.1645G= | ENSP00000264162.2:p.Ala549= | |
NM_002299.2:c.1645G= , LRG_338t1:c.1645G= | NP_002290.2:p.Ala549= | |
NM_002299.3:c.1645G= | NP_002290.2:p.Ala549= | |
XM_017004088.2:c.1645G= | XP_016859577.1:p.Ala549= | |
NM_002299.4:c.1645G= MANE Select | NP_002290.2:p.Ala549= |