HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48408641G>T , CM000677.2:g.48408641G>T | GRCh38 |
NC_000015.9:g.48700838G>T , CM000677.1:g.48700838G>T | GRCh37 |
NC_000015.8:g.46488130G>T | NCBI36 |
NG_008805.2:g.242148C>A , LRG_778:g.242148C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682170.1:n.5146C>A | ||
ENST00000682767.1:n.4262C>A | ||
ENST00000316623.10:c.*2349C>A MANE Select | ENSP00000325527.5:n.*2349C>A | |
ENST00000316623.9:c.*2349C>A | ENSP00000325527.5:n.*2349C>A | |
NM_000138.4:c.*2349C>A , LRG_778t1:c.*2349C>A | NP_000129.3:n.*2349C>A | |
NM_000138.5:c.*2349C>A MANE Select | NP_000129.3:n.*2349C>A |