HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70176023T>G , CM000679.2:g.70176023T>G | GRCh38 |
NC_000017.10:g.68172164T>G , CM000679.1:g.68172164T>G | GRCh37 |
NC_000017.9:g.65683759T>G | NCBI36 |
NG_008798.1:g.11489T>G , LRG_328:g.11489T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.984T>G MANE Select | ENSP00000243457.2:p.Pro328= | |
ENST00000243457.3:c.984T>G | ENSP00000243457.2:p.Pro328= | |
ENST00000535240.1:c.984T>G | ENSP00000441848.1:p.Pro328= | |
NM_000891.2:c.984T>G , LRG_328t1:c.984T>G | NP_000882.1:p.Pro328= | |
XM_011524779.1:c.984T>G | XP_011523081.1:p.Pro328= | |
NM_000891.3:c.984T>G MANE Select | NP_000882.1:p.Pro328= |