HGVS | Genome Assembly |
---|---|
NC_000014.9:g.60648621G= , CM000676.2:g.60648621G= | GRCh38 |
NC_000014.8:g.61115339G= , CM000676.1:g.61115339G= | GRCh37 |
NC_000014.7:g.60185092G= | NCBI36 |
NG_008231.1:g.5817C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645694.3:c.560+9C= MANE Select | ENSP00000494686.1:n.560+9C= | |
ENST00000247182.6:c.560+9C= | ENSP00000247182.5:n.560+9C= | |
ENST00000553535.2:n.249-2044C= | ||
ENST00000554986.2:c.42-2044C= | ENSP00000452700.2:n.42-2044C= | |
ENST00000555955.3:n.1198-2044C= | ||
NM_005982.3:c.560+9C= | NP_005973.1:n.560+9C= | |
XM_017021602.2:c.501+68C= | XP_016877091.1:n.501+68C= | |
NM_005982.4:c.560+9C= MANE Select | NP_005973.1:n.560+9C= |