HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8012166_8012167delinsAC , CM000679.2:g.8012166_8012167delinsAC | GRCh38 |
NC_000017.10:g.7915484_7915485delinsAC , CM000679.1:g.7915484_7915485delinsAC | GRCh37 |
NC_000017.9:g.7856209_7856210delinsAC | NCBI36 |
NG_009092.1:g.14497_14498delinsAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254854.5:c.1772_1773delinsAC MANE Select | ENSP00000254854.4:p.Asn591= | |
ENST00000254854.4:c.1772_1773delinsAC | ENSP00000254854.4:p.Asn591= | |
NM_000180.3:c.1772_1773delinsAC | NP_000171.1:p.Asn591= | |
XM_011523816.1:c.1772_1773delinsAC | XP_011522118.1:p.Asn591= | |
NM_000180.4:c.1772_1773delinsAC MANE Select | NP_000171.1:p.Asn591= |