HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48409527T>C , CM000677.2:g.48409527T>C | GRCh38 |
NC_000015.9:g.48701724T>C , CM000677.1:g.48701724T>C | GRCh37 |
NC_000015.8:g.46489016T>C | NCBI36 |
NG_008805.2:g.241262A>G , LRG_778:g.241262A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000682170.1:n.4260A>G | ||
ENST00000682767.1:n.3376A>G | ||
ENST00000316623.10:c.*1463A>G MANE Select | ENSP00000325527.5:n.*1463A>G | |
ENST00000316623.9:c.*1463A>G | ENSP00000325527.5:n.*1463A>G | |
NM_000138.4:c.*1463A>G , LRG_778t1:c.*1463A>G | NP_000129.3:n.*1463A>G | |
NM_000138.5:c.*1463A>G MANE Select | NP_000129.3:n.*1463A>G |