HGVS | Genome Assembly |
---|---|
NC_000002.12:g.184913711T= , CM000664.2:g.184913711T= | GRCh38 |
NC_000002.11:g.185778438T= , CM000664.1:g.185778438T= | GRCh37 |
NC_000002.10:g.185486683T= | NCBI36 |
NG_046950.1:g.320346T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000302277.7:c.256-19892T= MANE Select | ENSP00000303252.6:n.256-19892T= | |
ENST00000302277.6:c.256-19892T= | ENSP00000303252.6:n.256-19892T= | |
ENST00000613975.1:c.1-19892T= | ENSP00000483032.1:n.1-19892T= | |
NM_194250.1:c.256-19892T= | NP_919226.1:n.256-19892T= | |
NM_194250.2:c.256-19892T= MANE Select | NP_919226.1:n.256-19892T= |