HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63944723T>C , CM000679.2:g.63944723T>C | GRCh38 |
NC_000017.10:g.62022083T>C , CM000679.1:g.62022083T>C | GRCh37 |
NC_000017.9:g.59375815T>C | NCBI36 |
NG_011699.1:g.33196A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435607.3:c.3862A>G MANE Select | ENSP00000396320.1:p.Asn1288Asp | |
ENST00000578147.5:c.3862A>G | ENSP00000463963.1:p.Asn1288Asp | |
NM_000334.4:c.3862A>G MANE Select | NP_000325.4:p.Asn1288Asp | |
XM_005257566.3:c.3862A>G | XP_005257623.1:p.Asn1288Asp |