HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44160039T>C , CM000682.2:g.44160039T>C | GRCh38 |
NC_000020.10:g.42788679T>C , CM000682.1:g.42788679T>C | GRCh37 |
NC_000020.9:g.42222093T>C | NCBI36 |
NG_031867.1:g.32540A>G , LRG_394:g.32540A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372980.4:c.748A>G MANE Select | ENSP00000362071.3:p.Lys250Glu | |
ENST00000372980.3:c.748A>G | ENSP00000362071.3:p.Lys250Glu | |
NM_020433.4:c.748A>G , LRG_394t1:c.748A>G | NP_065166.2:p.Lys250Glu | |
XM_006723832.2:c.748A>G | XP_006723895.1:p.Lys250Glu | |
NM_020433.5:c.748A>G MANE Select | NP_065166.2:p.Lys250Glu |