HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60645454C= , CM000676.2:g.60645454C= | GRCh38 |
NC_000014.8:g.61112172C= , CM000676.1:g.61112172C= | GRCh37 |
NC_000014.7:g.60181925C= | NCBI36 |
NG_008231.1:g.8984G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000645694.3:c.*829G= MANE Select | ENSP00000494686.1:n.*829G= | |
ENST00000247182.6:c.*829G= | ENSP00000247182.5:n.*829G= | |
ENST00000553535.2:n.1372G= | ||
ENST00000554986.2:c.*829G= | ENSP00000452700.2:n.*829G= | |
ENST00000555955.3:n.2321G= | ||
NM_005982.3:c.*829G= | NP_005973.1:n.*829G= | |
XM_017021602.2:c.*1103G= | XP_016877091.1:n.*1103G= | |
NM_005982.4:c.*829G= MANE Select | NP_005973.1:n.*829G= |