HGVS | Genome Assembly |
---|---|
NC_000003.12:g.52224163C>T , CM000665.2:g.52224163C>T | GRCh38 |
NC_000003.11:g.52258179C>T , CM000665.1:g.52258179C>T | GRCh37 |
NC_000003.10:g.52233219C>T | NCBI36 |
NG_033933.1:g.7001G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360658.3:c.153G>A MANE Select | ENSP00000353874.2:p.Lys51= | |
ENST00000360658.2:c.153G>A | ENSP00000353874.2:p.Lys51= | |
ENST00000478201.1:c.327G>A | ||
ENST00000494383.1:c.613G>A | ||
NM_017442.3:c.153G>A | NP_059138.1:p.Lys51= | |
NM_017442.4:c.153G>A MANE Select | NP_059138.1:p.Lys51= |