HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028771C= , CM000667.2:g.135028771C= | GRCh38 |
NC_000005.9:g.134364461C= , CM000667.1:g.134364461C= | GRCh37 |
NC_000005.8:g.134392360C= | NCBI36 |
NG_012114.1:g.10504G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.*8G= MANE Select | ENSP00000265340.6:n.*8G= | |
ENST00000265340.11:c.*8G= | ENSP00000265340.6:n.*8G= | |
ENST00000506438.5:c.*8G= | ENSP00000427542.1:n.*8G= | |
NM_002653.4:c.*8G= | NP_002644.4:n.*8G= | |
NM_002653.5:c.*8G= MANE Select | NP_002644.4:n.*8G= |