HGVS | Genome Assembly |
---|---|
NC_000004.12:g.40354291_40354292delinsTG , CM000666.2:g.40354291_40354292delinsTG | GRCh38 |
NC_000004.11:g.40356308_40356309delinsTG , CM000666.1:g.40356308_40356309delinsTG | GRCh37 |
NC_000004.10:g.40051065_40051066delinsTG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310169.3:c.1211_1212delinsTG MANE Select | ENSP00000312663.2:p.Leu404= | |
ENST00000310169.2:c.1211_1212delinsTG | ENSP00000312663.2:p.Leu404= | |
NM_017581.3:c.1211_1212delinsTG | NP_060051.2:p.Leu404= | |
NM_017581.4:c.1211_1212delinsTG MANE Select | NP_060051.2:p.Leu404= |