HGVS | Genome Assembly |
---|---|
NC_000019.10:g.33302356T= , CM000681.2:g.33302356T= | GRCh38 |
NC_000019.9:g.33793262T= , CM000681.1:g.33793262T= | GRCh37 |
NC_000019.8:g.38485102T= | NCBI36 |
NG_012022.1:g.5169A= , LRG_456:g.5169A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000498907.3:c.59A= MANE Select | ENSP00000427514.1:p.Gln20= | |
ENST00000498907.2:c.59A= | ENSP00000427514.1:p.Gln20= | |
NM_001285829.1:c.-299A= | NP_001272758.1:n.-299A= | |
NM_001287424.1:c.164A= | NP_001274353.1:p.Gln55= | |
NM_001287435.1:c.17A= | NP_001274364.1:p.Gln6= | |
NM_004364.4:c.59A= | NP_004355.2:p.Gln20= | |
NM_001287424.2:c.164A= | NP_001274353.1:p.Gln55= | |
NM_004364.5:c.59A= MANE Select | NP_004355.2:p.Gln20= | |
NM_001285829.2:c.-299A= | NP_001272758.1:n.-299A= | |
NM_001287435.2:c.17A= | NP_001274364.1:p.Gln6= |