HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186194628T= , CM000666.2:g.186194628T= | GRCh38 |
NC_000004.11:g.187115782T= , CM000666.1:g.187115782T= | GRCh37 |
NC_000004.10:g.187352776T= | NCBI36 |
NG_007965.1:g.8109T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378802.5:c.327+16T= MANE Select | ENSP00000368079.4:n.327+16T= | |
ENST00000378802.4:c.327+16T= | ENSP00000368079.4:n.327+16T= | |
NM_207352.3:c.327+16T= | NP_997235.3:n.327+16T= | |
XM_005262935.2:c.327+16T= | XP_005262992.1:n.327+16T= | |
XM_006714184.2:c.17+16T= | XP_006714247.1:n.17+16T= | |
XM_005262935.4:c.327+16T= | XP_005262992.1:n.327+16T= | |
XM_017008037.1:c.17+16T= | XP_016863526.1:n.17+16T= | |
NM_207352.4:c.327+16T= MANE Select | NP_997235.3:n.327+16T= |