HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120739318_120739319delinsTG , CM000674.2:g.120739318_120739319delinsTG | GRCh38 |
NC_000012.11:g.121177121_121177122delinsTG , CM000674.1:g.121177121_121177122delinsTG | GRCh37 |
NC_000012.10:g.119661504_119661505delinsTG | NCBI36 |
NG_007991.1:g.18551_18552delinsTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000242592.9:c.1109_1110delinsTG MANE Select | ENSP00000242592.4:p.Met370= | |
ENST00000242592.8:c.1109_1110delinsTG | ENSP00000242592.4:p.Met370= | |
ENST00000411593.2:c.1097_1098delinsTG | ENSP00000401045.2:p.Met366= | |
NM_000017.3:c.1109_1110delinsTG | NP_000008.1:p.Met370= | |
NM_001302554.1:c.1097_1098delinsTG | NP_001289483.1:p.Met366= | |
NM_000017.4:c.1109_1110delinsTG MANE Select | NP_000008.1:p.Met370= | |
NM_001302554.2:c.1097_1098delinsTG | NP_001289483.1:p.Met366= |