HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28768470T>A , CM000676.2:g.28768470T>A | GRCh38 |
NC_000014.8:g.29237676T>A , CM000676.1:g.29237676T>A | GRCh37 |
NC_000014.7:g.28307427T>A | NCBI36 |
NG_009367.1:g.6390T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.1191T>A | ENSP00000516406.1:p.Ser397= | |
ENST00000313071.7:c.1191T>A MANE Select | ENSP00000339004.3:p.Ser397= | |
ENST00000313071.6:c.1191T>A | ENSP00000339004.3:p.Ser397= | |
NM_005249.4:c.1191T>A | NP_005240.3:p.Ser397= | |
NM_005249.5:c.1191T>A MANE Select | NP_005240.3:p.Ser397= |