HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94849927T= , CM000672.2:g.94849927T= | GRCh38 |
NC_000010.10:g.96609684T= , CM000672.1:g.96609684T= | GRCh37 |
NC_000010.9:g.96599674T= | NCBI36 |
NG_008384.2:g.92222T= | |
NG_008384.3:g.92247T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.1160T= MANE Select | ENSP00000360372.3:p.Ile387= | |
ENST00000645461.1:n.2071T= | ||
ENST00000371321.7:c.1160T= | ENSP00000360372.3:p.Ile387= | |
ENST00000464755.1:c.1923T= | ENSP00000483243.1:n.1923T= | |
NM_000769.2:c.1160T= | NP_000760.1:p.Ile387= | |
NM_000769.4:c.1160T= MANE Select | NP_000760.1:p.Ile387= |