HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48409192T= , CM000677.2:g.48409192T= | GRCh38 |
NC_000015.9:g.48701389T= , CM000677.1:g.48701389T= | GRCh37 |
NC_000015.8:g.46488681T= | NCBI36 |
NG_008805.2:g.241597A= , LRG_778:g.241597A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682170.1:n.4595A= | ||
ENST00000682767.1:n.3711A= | ||
ENST00000316623.10:c.*1798A= MANE Select | ENSP00000325527.5:n.*1798A= | |
ENST00000316623.9:c.*1798A= | ENSP00000325527.5:n.*1798A= | |
NM_000138.4:c.*1798A= , LRG_778t1:c.*1798A= | NP_000129.3:n.*1798A= | |
NM_000138.5:c.*1798A= MANE Select | NP_000129.3:n.*1798A= |