HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186197665C= , CM000666.2:g.186197665C= | GRCh38 |
NC_000004.11:g.187118819C= , CM000666.1:g.187118819C= | GRCh37 |
NC_000004.10:g.187355813C= | NCBI36 |
NG_007965.1:g.11146C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378802.5:c.674+63C= MANE Select | ENSP00000368079.4:n.674+63C= | |
ENST00000378802.4:c.674+63C= | ENSP00000368079.4:n.674+63C= | |
ENST00000507209.5:n.1515+63C= | ||
NM_207352.3:c.674+63C= | NP_997235.3:n.674+63C= | |
XM_005262935.2:c.674+63C= | XP_005262992.1:n.674+63C= | |
XM_006714184.2:c.278+63C= | XP_006714247.1:n.278+63C= | |
XM_005262935.4:c.674+63C= | XP_005262992.1:n.674+63C= | |
XM_017008037.1:c.278+63C= | XP_016863526.1:n.278+63C= | |
NM_207352.4:c.674+63C= MANE Select | NP_997235.3:n.674+63C= |