HGVS | Genome Assembly |
---|---|
NC_000014.9:g.93218560T>C , CM000676.2:g.93218560T>C | GRCh38 |
NC_000014.8:g.93684906T>C , CM000676.1:g.93684906T>C | GRCh37 |
NC_000014.7:g.92754659T>C | NCBI36 |
NG_051089.1:g.16505T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000013070.11:c.635T>C MANE Select | ENSP00000013070.6:p.Val212Ala | |
ENST00000013070.10:c.635T>C | ENSP00000013070.6:p.Val212Ala | |
ENST00000416753.5:c.407T>C | ENSP00000391706.2:p.Val136Ala | |
ENST00000553674.1:c.*336T>C | ENSP00000450470.1:n.*336T>C | |
ENST00000553857.5:c.378+3279T>C | ||
ENST00000556871.5:c.344T>C | ENSP00000451022.1:p.Val115Ala | |
ENST00000557048.1:n.544T>C | ||
NM_175748.3:c.635T>C | NP_786924.2:p.Val212Ala | |
NR_038150.1:n.737T>C | ||
NM_175748.4:c.635T>C MANE Select | NP_786924.2:p.Val212Ala | |
NR_038150.2:n.537T>C |