HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134750798T= , CM000671.2:g.134750798T= | GRCh38 |
NC_000009.11:g.137642644T= , CM000671.1:g.137642644T= | GRCh37 |
NC_000009.10:g.136782465T= | NCBI36 |
NG_008030.1:g.113993T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371820.4:c.1578T= | ENSP00000360885.4:p.Phe526= | |
ENST00000371817.8:c.1578T= MANE Select | ENSP00000360882.3:p.Phe526= | |
ENST00000371817.7:c.1578T= | ENSP00000360882.3:p.Phe526= | |
ENST00000618395.4:c.1578T= | ENSP00000481360.1:p.Phe526= | |
NM_000093.4:c.1578T= | NP_000084.3:p.Phe526= | |
NM_001278074.1:c.1578T= | NP_001265003.1:p.Phe526= | |
XR_929712.1:n.1980T= | ||
XR_929713.1:n.1980T= | ||
XM_017014266.2:c.1578T= | XP_016869755.1:p.Phe526= | |
XR_001746183.1:n.1976T= | ||
NM_000093.5:c.1578T= MANE Select | NP_000084.3:p.Phe526= |