HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154903530T>C , CM000685.2:g.154903530T>C | GRCh38 |
NC_000023.10:g.154131805T>C , CM000685.1:g.154131805T>C | GRCh37 |
NC_000023.9:g.153784999T>C | NCBI36 |
NG_011403.1:g.124194A>G | |
NG_011403.2:g.124194A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5998+376A>G MANE Select | ENSP00000353393.4:n.5998+376A>G | |
ENST00000360256.8:c.5998+376A>G | ENSP00000353393.4:n.5998+376A>G | |
NM_000132.3:c.5998+376A>G | NP_000123.1:n.5998+376A>G | |
XM_011531126.1:c.5893+376A>G | XP_011529428.1:n.5893+376A>G | |
NM_000132.4:c.5998+376A>G MANE Select | NP_000123.1:n.5998+376A>G |