HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339721G>T , CM000669.2:g.17339721G>T | GRCh38 |
NC_000007.13:g.17379345G>T , CM000669.1:g.17379345G>T | GRCh37 |
NC_000007.12:g.17345870G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1896G>T MANE Select | ENSP00000242057.4:p.Val632= | |
ENST00000637807.1:c.1866G>T | ENSP00000490530.1:p.Val622= | |
ENST00000642825.1:c.1851G>T | ENSP00000495987.1:p.Val617= | |
ENST00000242057.8:c.1896G>T | ENSP00000242057.4:p.Val632= | |
ENST00000463496.1:c.1896G>T | ENSP00000436466.1:p.Val632= | |
NM_001621.4:c.1896G>T | NP_001612.1:p.Val632= | |
NM_001621.5:c.1896G>T MANE Select | NP_001612.1:p.Val632= |