HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670145A>C , CM000666.2:g.68670145A>C | GRCh38 |
NC_000004.11:g.69535863A>C , CM000666.1:g.69535863A>C | GRCh37 |
NC_000004.10:g.69218458A>C | NCBI36 |
NG_052676.1:g.5632T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.474T>G MANE Select | ENSP00000341045.5:p.Gly158= | |
ENST00000338206.5:c.474T>G | ENSP00000341045.5:p.Gly158= | |
ENST00000616841.4:c.474T>G | ENSP00000482004.1:p.Gly158= | |
NM_001076.3:c.474T>G | NP_001067.2:p.Gly158= | |
NM_001076.4:c.474T>G MANE Select | NP_001067.2:p.Gly158= |