HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713907_114713908delinsTT , CM000663.2:g.114713907_114713908delinsTT | GRCh38 |
NC_000001.10:g.115256528_115256529delinsTT , CM000663.1:g.115256528_115256529delinsTT | GRCh37 |
NC_000001.9:g.115058051_115058052delinsTT | NCBI36 |
NG_007572.1:g.7987_7988delinsAA , LRG_92:g.7987_7988delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.182_183delinsAA MANE Select | ENSP00000358548.4:p.Gln61= | |
ENST00000369535.4:c.182_183delinsAA | ENSP00000358548.4:p.Gln61= | |
NM_002524.4:c.182_183delinsAA | NP_002515.1:p.Gln61= | |
NM_002524.5:c.182_183delinsAA MANE Select | NP_002515.1:p.Gln61= |