HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23415083_23415084delinsTT , CM000676.2:g.23415083_23415084delinsTT | GRCh38 |
NC_000014.8:g.23884292_23884293delinsTT , CM000676.1:g.23884292_23884293delinsTT | GRCh37 |
NC_000014.7:g.22954132_22954133delinsTT | NCBI36 |
NG_007884.1:g.25578_25579delinsAA , LRG_384:g.25578_25579delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.5470_5471delinsAA MANE Select | ENSP00000347507.3:p.Asn1824= | |
ENST00000355349.3:c.5470_5471delinsAA | ENSP00000347507.3:p.Asn1824= | |
NM_000257.3:c.5470_5471delinsAA | NP_000248.2:p.Asn1824= | |
XM_017021340.1:c.5470_5471delinsAA | XP_016876829.1:p.Asn1824= | |
NM_000257.4:c.5470_5471delinsAA MANE Select | NP_000248.2:p.Asn1824= |