HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48410681T>G , CM000677.2:g.48410681T>G | GRCh38 |
NC_000015.9:g.48702878T>G , CM000677.1:g.48702878T>G | GRCh37 |
NC_000015.8:g.46490170T>G | NCBI36 |
NG_008805.2:g.240108A>C , LRG_778:g.240108A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.*1733A>C | ENSP00000453958.2:n.*1733A>C | |
ENST00000682158.1:n.2306A>C | ||
ENST00000682170.1:n.3106A>C | ||
ENST00000682767.1:n.2222A>C | ||
ENST00000316623.10:c.*309A>C MANE Select | ENSP00000325527.5:n.*309A>C | |
ENST00000316623.9:c.*309A>C | ENSP00000325527.5:n.*309A>C | |
ENST00000559133.5:c.4294A>C | ||
NM_000138.4:c.*309A>C , LRG_778t1:c.*309A>C | NP_000129.3:n.*309A>C | |
NM_000138.5:c.*309A>C MANE Select | NP_000129.3:n.*309A>C |