HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583618C= , CM000679.2:g.41583618C= | GRCh38 |
NC_000017.10:g.39739870C= , CM000679.1:g.39739870C= | GRCh37 |
NC_000017.9:g.36993396C= | NCBI36 |
NG_008624.1:g.8278G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.986G= MANE Select | ENSP00000167586.6:p.Ser329= | |
ENST00000167586.6:c.986G= | ENSP00000167586.6:p.Ser329= | |
ENST00000476662.1:n.436G= | ||
NM_000526.4:c.986G= | NP_000517.2:p.Ser329= | |
NM_000526.5:c.986G= MANE Select | NP_000517.3:p.Ser329= |