HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153737252G>C , CM000685.2:g.153737252G>C | GRCh38 |
NC_000023.10:g.153002706G>C , CM000685.1:g.153002706G>C | GRCh37 |
NC_000023.9:g.152655900G>C | NCBI36 |
NG_009022.2:g.17385G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1488+1G>C MANE Select | ENSP00000218104.3:n.1488+1G>C | |
ENST00000218104.5:c.1488+1G>C | ENSP00000218104.3:n.1488+1G>C | |
ENST00000443684.2:n.491+1G>C | ||
NM_000033.3:c.1488+1G>C | NP_000024.2:n.1488+1G>C | |
XR_938507.1:n.1960+1G>C | ||
XR_938507.2:n.1960+1G>C | ||
NM_000033.4:c.1488+1G>C MANE Select | NP_000024.2:n.1488+1G>C |