HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48410721C>T , CM000677.2:g.48410721C>T | GRCh38 |
NC_000015.9:g.48702918C>T , CM000677.1:g.48702918C>T | GRCh37 |
NC_000015.8:g.46490210C>T | NCBI36 |
NG_008805.2:g.240068G>A , LRG_778:g.240068G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1693G>A | ENSP00000453958.2:n.*1693G>A | |
ENST00000682158.1:n.2266G>A | ||
ENST00000682170.1:n.3066G>A | ||
ENST00000682767.1:n.2182G>A | ||
ENST00000316623.10:c.*269G>A MANE Select | ENSP00000325527.5:n.*269G>A | |
ENST00000316623.9:c.*269G>A | ENSP00000325527.5:n.*269G>A | |
ENST00000559133.5:c.4254G>A | ||
NM_000138.4:c.*269G>A , LRG_778t1:c.*269G>A | NP_000129.3:n.*269G>A | |
NM_000138.5:c.*269G>A MANE Select | NP_000129.3:n.*269G>A |