HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160130591C>T , CM000663.2:g.160130591C>T | GRCh38 |
NC_000001.10:g.160100381C>T , CM000663.1:g.160100381C>T | GRCh37 |
NC_000001.9:g.158367005C>T | NCBI36 |
NG_008014.1:g.19834C>T , LRG_6:g.19834C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361216.8:c.1821C>T MANE Select | ENSP00000354490.3:p.Gly607= | |
ENST00000361216.7:c.1821C>T | ENSP00000354490.3:p.Gly607= | |
ENST00000392233.7:c.1821C>T | ENSP00000376066.3:p.Gly607= | |
ENST00000447527.1:c.953C>T | ||
ENST00000472488.5:n.1924C>T | ||
NM_000702.3:c.1821C>T | NP_000693.1:p.Gly607= | |
NM_000702.4:c.1821C>T MANE Select | NP_000693.1:p.Gly607= |