HGVS | Genome Assembly |
---|---|
NC_000017.11:g.50196332A= , CM000679.2:g.50196332A= | GRCh38 |
NC_000017.10:g.48273693A= , CM000679.1:g.48273693A= | GRCh37 |
NC_000017.9:g.45628692A= | NCBI36 |
NG_007400.1:g.10308T= , LRG_1:g.10308T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225964.10:c.939T= MANE Select | ENSP00000225964.6:p.Pro313= | |
ENST00000225964.9:c.939T= | ENSP00000225964.5:p.Pro313= | |
ENST00000485870.1:n.264T= | ||
NM_000088.3:c.939T= , LRG_1t1:c.939T= | NP_000079.2:p.Pro313= | |
XM_005257058.3:c.939T= | XP_005257115.2:p.Pro313= | |
XM_005257059.3:c.939T= | XP_005257116.2:p.Pro313= | |
XM_011524341.1:c.939T= | XP_011522643.1:p.Pro313= | |
XM_005257058.4:c.939T= | XP_005257115.2:p.Pro313= | |
XM_005257059.4:c.939T= | XP_005257116.2:p.Pro313= | |
NM_000088.4:c.939T= MANE Select | NP_000079.2:p.Pro313= |