HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154904049A>T , CM000685.2:g.154904049A>T | GRCh38 |
NC_000023.10:g.154132324A>T , CM000685.1:g.154132324A>T | GRCh37 |
NC_000023.9:g.153785518A>T | NCBI36 |
NG_011403.1:g.123675T>A | |
NG_011403.2:g.123675T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5855T>A MANE Select | ENSP00000353393.4:p.Val1952Glu | |
ENST00000360256.8:c.5855T>A | ENSP00000353393.4:p.Val1952Glu | |
NM_000132.3:c.5855T>A | NP_000123.1:p.Val1952Glu | |
XM_011531126.1:c.5750T>A | XP_011529428.1:p.Val1917Glu | |
NM_000132.4:c.5855T>A MANE Select | NP_000123.1:p.Val1952Glu |