HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44118550C>A , CM000682.2:g.44118550C>A | GRCh38 |
NC_000020.10:g.42747190C>A , CM000682.1:g.42747190C>A | GRCh37 |
NC_000020.9:g.42180604C>A | NCBI36 |
NG_031867.1:g.74029G>T , LRG_394:g.74029G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372980.4:c.1243G>T MANE Select | ENSP00000362071.3:p.Ala415Ser | |
ENST00000372980.3:c.1243G>T | ENSP00000362071.3:p.Ala415Ser | |
NM_020433.4:c.1243G>T , LRG_394t1:c.1243G>T | NP_065166.2:p.Ala415Ser | |
XM_006723832.2:c.1243G>T | XP_006723895.1:p.Ala415Ser | |
NM_020433.5:c.1243G>T MANE Select | NP_065166.2:p.Ala415Ser |