HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21704474T= , CM000669.2:g.21704474T= | GRCh38 |
NC_000007.13:g.21744092T= , CM000669.1:g.21744092T= | GRCh37 |
NC_000007.12:g.21710617T= | NCBI36 |
NG_012886.2:g.166260T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000409508.8:c.6314T= MANE Select | ENSP00000475939.1:p.Ile2105= | |
ENST00000328843.10:c.6335T= | ENSP00000330671.7:p.Ile2112= | |
ENST00000409508.7:c.6314T= | ENSP00000475939.1:p.Ile2105= | |
ENST00000620169.4:c.6335T= | ENSP00000481693.1:p.Ile2112= | |
NM_001277115.1:c.6314T= | NP_001264044.1:p.Ile2105= | |
NM_001277115.2:c.6314T= MANE Select | NP_001264044.1:p.Ile2105= |