HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028730C= , CM000667.2:g.135028730C= | GRCh38 |
NC_000005.9:g.134364420C= , CM000667.1:g.134364420C= | GRCh37 |
NC_000005.8:g.134392319C= | NCBI36 |
NG_012114.1:g.10545G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.*49G= MANE Select | ENSP00000265340.6:n.*49G= | |
ENST00000265340.11:c.*49G= | ENSP00000265340.6:n.*49G= | |
ENST00000506438.5:c.*49G= | ENSP00000427542.1:n.*49G= | |
NM_002653.4:c.*49G= | NP_002644.4:n.*49G= | |
NM_002653.5:c.*49G= MANE Select | NP_002644.4:n.*49G= |