HGVS | Genome Assembly |
---|---|
NC_000007.14:g.87503861A= , CM000669.2:g.87503861A= | GRCh38 |
NC_000007.13:g.87133177A= , CM000669.1:g.87133177A= | GRCh37 |
NC_000007.12:g.86971113A= | NCBI36 |
NG_011513.1:g.214388T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000265724.8:c.*382T= | ENSP00000265724.3:n.*382T= | |
ENST00000622132.5:c.*382T= MANE Select | ENSP00000478255.1:n.*382T= | |
ENST00000265724.7:c.*382T= | ENSP00000265724.3:n.*382T= | |
ENST00000622132.4:c.*382T= | ENSP00000478255.1:n.*382T= | |
NM_001348946.2:c.*382T= MANE Select | NP_001335875.1:n.*382T= | |
NM_000927.5:c.*382T= | NP_000918.2:n.*382T= | |
NM_001348944.2:c.*382T= | NP_001335873.1:n.*382T= | |
NM_001348945.2:c.*382T= | NP_001335874.1:n.*382T= |