HGVS | Genome Assembly |
---|---|
NC_000010.11:g.85980942T>A , CM000672.2:g.85980942T>A | GRCh38 |
NC_000010.10:g.87740699T>A , CM000672.1:g.87740699T>A | GRCh37 |
NC_000010.9:g.87730679T>A | NCBI36 |
NG_011875.1:g.390552A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327946.12:c.727-64703A>T MANE Select | ENSP00000330148.7:n.727-64703A>T | |
ENST00000327946.11:c.727-64703A>T | ENSP00000330148.7:n.727-64703A>T | |
ENST00000464741.2:c.727-64703A>T | ENSP00000433064.1:n.727-64703A>T | |
NM_017551.2:c.727-64703A>T | NP_060021.1:n.727-64703A>T | |
XM_011539720.1:c.727-64703A>T | XP_011538022.1:n.727-64703A>T | |
XM_011539720.2:c.727-64703A>T | XP_011538022.1:n.727-64703A>T | |
NM_017551.3:c.727-64703A>T MANE Select | NP_060021.1:n.727-64703A>T |