HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21558633T= , CM000669.2:g.21558633T= | GRCh38 |
NC_000007.13:g.21598251T= , CM000669.1:g.21598251T= | GRCh37 |
NC_000007.12:g.21564776T= | NCBI36 |
NG_012886.2:g.20419T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.496-169T= MANE Select | ENSP00000475939.1:n.496-169T= | |
ENST00000328843.10:c.496-169T= | ENSP00000330671.7:n.496-169T= | |
ENST00000409508.7:c.496-169T= | ENSP00000475939.1:n.496-169T= | |
ENST00000620169.4:c.496-169T= | ENSP00000481693.1:n.496-169T= | |
NM_001277115.1:c.496-169T= | NP_001264044.1:n.496-169T= | |
NM_001277115.2:c.496-169T= MANE Select | NP_001264044.1:n.496-169T= |