HGVS | Genome Assembly |
---|---|
NC_000001.11:g.37812997T>C , CM000663.2:g.37812997T>C | GRCh38 |
NC_000001.10:g.38278669T>C , CM000663.1:g.38278669T>C | GRCh37 |
NC_000001.9:g.38051256T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373036.5:c.*2139A>G MANE Select | ENSP00000362127.3:n.*2139A>G | |
ENST00000373036.4:c.*2139A>G | ENSP00000362127.3:n.*2139A>G | |
NM_005955.2:c.*2139A>G | NP_005946.2:n.*2139A>G | |
XM_011541491.1:c.*2139A>G | XP_011539793.1:n.*2139A>G | |
XM_011541492.1:c.*2139A>G | XP_011539794.1:n.*2139A>G | |
XM_011541494.1:c.*2139A>G | XP_011539796.1:n.*2139A>G | |
XM_011541491.2:c.*2139A>G | XP_011539793.1:n.*2139A>G | |
NM_005955.3:c.*2139A>G MANE Select | NP_005946.2:n.*2139A>G |