HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884939_13884941delinsCAT , CM000680.2:g.13884939_13884941delinsCAT | GRCh38 |
NC_000018.9:g.13884938_13884940delinsCAT , CM000680.1:g.13884938_13884940delinsCAT | GRCh37 |
NC_000018.8:g.13874938_13874940delinsCAT | NCBI36 |
NG_011819.1:g.35596_35598delinsATG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327606.4:c.578_580delinsATG MANE Select | ENSP00000333821.2:p.Tyr193= | |
ENST00000327606.3:c.578_580delinsATG | ENSP00000333821.2:p.Tyr193= | |
NM_000529.2:c.578_580delinsATG MANE Select | NP_000520.1:p.Tyr193= | |
NM_001291911.1:c.578_580delinsATG | NP_001278840.1:p.Tyr193= | |
XM_017025781.1:c.578_580delinsATG | XP_016881270.1:p.Tyr193= |