HGVS | Genome Assembly |
---|---|
NC_000017.11:g.15999695G= , CM000679.2:g.15999695G= | GRCh38 |
NC_000017.10:g.15903009G= , CM000679.1:g.15903009G= | GRCh37 |
NC_000017.9:g.15843734G= | NCBI36 |
NG_029806.1:g.5316G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000399277.6:c.-101C= (ZSWIM7) MANE Select | ENSP00000382218.1:n.-101C= | |
ENST00000261647.9:c.-154G= (TTC19) | ENSP00000261647.5:n.-154G= | |
ENST00000491631.5:c.-101C= (ZSWIM7) | ENSP00000462598.1:n.-101C= | |
ENST00000497719.5:n.19C= (ZSWIM7) | ||
NM_001271420.1:c.-612G= (TTC19) | NP_001258349.1:n.-612G= | |
NM_017775.3:c.-154G= (TTC19) | NP_060245.3:n.-154G= | |
NM_001042697.2:c.-101C= (ZSWIM7) MANE Select | NP_001036162.1:n.-101C= | |
NM_001042698.2:c.-101C= (ZSWIM7) | NP_001036163.1:n.-101C= |