HGVS | Genome Assembly |
---|---|
NC_000007.14:g.87600187C= , CM000669.2:g.87600187C= | GRCh38 |
NC_000007.13:g.87229503C= , CM000669.1:g.87229503C= | GRCh37 |
NC_000007.12:g.87067439C= | NCBI36 |
NG_011513.1:g.118062G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265724.8:c.-3G= | ENSP00000265724.3:n.-3G= | |
ENST00000622132.5:c.-3G= MANE Select | ENSP00000478255.1:n.-3G= | |
ENST00000265724.7:c.-3G= | ENSP00000265724.3:n.-3G= | |
ENST00000416177.1:c.-3G= | ENSP00000399419.1:n.-3G= | |
ENST00000543898.5:c.-3G= | ENSP00000444095.1:n.-3G= | |
ENST00000622132.4:c.-3G= | ENSP00000478255.1:n.-3G= | |
NM_000927.4:c.-3G= | NP_000918.2:n.-3G= | |
NM_001348944.1:c.-3G= | NP_001335873.1:n.-3G= | |
NM_001348945.1:c.208G= | NP_001335874.1:p.Gly70= | |
NM_001348946.1:c.-3G= | NP_001335875.1:n.-3G= | |
NM_001348946.2:c.-3G= MANE Select | NP_001335875.1:n.-3G= | |
NM_000927.5:c.-3G= | NP_000918.2:n.-3G= | |
NM_001348944.2:c.-3G= | NP_001335873.1:n.-3G= | |
NM_001348945.2:c.208G= | NP_001335874.1:p.Gly70= |