HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48408650T>G , CM000677.2:g.48408650T>G | GRCh38 |
NC_000015.9:g.48700847T>G , CM000677.1:g.48700847T>G | GRCh37 |
NC_000015.8:g.46488139T>G | NCBI36 |
NG_008805.2:g.242139A>C , LRG_778:g.242139A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682170.1:n.5137A>C | ||
ENST00000682767.1:n.4253A>C | ||
ENST00000316623.10:c.*2340A>C MANE Select | ENSP00000325527.5:n.*2340A>C | |
ENST00000316623.9:c.*2340A>C | ENSP00000325527.5:n.*2340A>C | |
NM_000138.4:c.*2340A>C , LRG_778t1:c.*2340A>C | NP_000129.3:n.*2340A>C | |
NM_000138.5:c.*2340A>C MANE Select | NP_000129.3:n.*2340A>C |