HGVS | Genome Assembly |
---|---|
NC_000006.12:g.38696994C= , CM000668.2:g.38696994C= | GRCh38 |
NC_000006.11:g.38664770C= , CM000668.1:g.38664770C= | GRCh37 |
NC_000006.10:g.38772748C= | NCBI36 |
NG_012074.1:g.11183G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373365.5:c.84+5977G= MANE Select | ENSP00000362463.3:n.84+5977G= | |
ENST00000373365.4:c.84+5977G= | ENSP00000362463.3:n.84+5977G= | |
NM_006708.2:c.84+5977G= | NP_006699.2:n.84+5977G= | |
NM_006708.3:c.84+5977G= MANE Select | NP_006699.2:n.84+5977G= |