HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47733456_47733457delinsTG , CM000679.2:g.47733456_47733457delinsTG | GRCh38 |
NC_000017.10:g.45810822_45810823delinsTG , CM000679.1:g.45810822_45810823delinsTG | GRCh37 |
NC_000017.9:g.43165821_43165822delinsTG | NCBI36 |
NG_012166.1:g.5213_5214delinsTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000177694.2:c.2_3delinsTG MANE Select | ENSP00000177694.1:p.Met1= | |
ENST00000177694.1:c.2_3delinsTG | ENSP00000177694.1:p.Met1= | |
ENST00000581328.1:n.32_33delinsTG | ||
NM_013351.1:c.2_3delinsTG | NP_037483.1:p.Met1= | |
XM_011524698.1:c.2_3delinsTG | XP_011523000.1:p.Met1= | |
NM_013351.2:c.2_3delinsTG MANE Select | NP_037483.1:p.Met1= |