HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877877C= , CM000670.2:g.6877877C= | GRCh38 |
NC_000008.10:g.6735399C= , CM000670.1:g.6735399C= | GRCh37 |
NC_000008.9:g.6722809C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297439.4:c.-20G= MANE Select | ENSP00000297439.3:n.-20G= | |
ENST00000297439.3:c.-20G= | ENSP00000297439.3:n.-20G= | |
NM_005218.3:c.-20G= | NP_005209.1:n.-20G= | |
NM_005218.4:c.-20G= MANE Select | NP_005209.1:n.-20G= |