HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400385_18400386delinsTC , CM000670.2:g.18400385_18400386delinsTC | GRCh38 |
NC_000008.10:g.18257895_18257896delinsTC , CM000670.1:g.18257895_18257896delinsTC | GRCh37 |
NC_000008.9:g.18302175_18302176delinsTC | NCBI36 |
NG_012246.1:g.14141_14142delinsTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286479.4:c.382_383delinsTC MANE Select | ENSP00000286479.3:p.Ser128= | |
ENST00000286479.3:c.382_383delinsTC | ENSP00000286479.3:p.Ser128= | |
ENST00000520116.1:c.-9_-8delinsTC | ENSP00000428416.1:n.-9_-8delinsTC | |
NM_000015.2:c.382_383delinsTC | NP_000006.2:p.Ser128= | |
XM_011544358.1:c.382_383delinsTC | XP_011542660.1:p.Ser128= | |
XM_017012938.1:c.382_383delinsTC | XP_016868427.1:p.Ser128= | |
NM_000015.3:c.382_383delinsTC MANE Select | NP_000006.2:p.Ser128= |