HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32220579C= , CM000668.2:g.32220579C= | GRCh38 |
NC_000006.11:g.32188356C= , CM000668.1:g.32188356C= | GRCh37 |
NC_000006.10:g.32296334C= | NCBI36 |
NG_028190.1:g.8489G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.985G= MANE Select | ENSP00000364163.3:p.Gly329= | |
ENST00000473562.1:n.1114G= | ||
NM_004557.3:c.985G= | NP_004548.3:p.Gly329= | |
NR_134949.1:n.1124G= | ||
NR_134950.1:n.1124G= | ||
NM_004557.4:c.985G= MANE Select | NP_004548.3:p.Gly329= | |
NR_134949.2:n.1124G= | ||
NR_134950.2:n.1124G= |