HGVS | Genome Assembly |
---|---|
NC_000002.12:g.70831759T>A , CM000664.2:g.70831759T>A | GRCh38 |
NC_000002.11:g.71058890T>A , CM000664.1:g.71058890T>A | GRCh37 |
NC_000002.10:g.70912398T>A | NCBI36 |
NG_033914.1:g.9065A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000410009.5:c.778A>T MANE Select | ENSP00000386378.3:p.Met260Leu | |
ENST00000410009.4:c.778A>T | ENSP00000386378.3:p.Met260Leu | |
NM_015717.4:c.778A>T | NP_056532.4:p.Met260Leu | |
XM_011532874.1:c.778A>T | XP_011531176.1:p.Met260Leu | |
XM_011532875.1:c.778A>T | XP_011531177.1:p.Met260Leu | |
XM_011532876.1:c.778A>T | XP_011531178.1:p.Met260Leu | |
XM_011532875.2:c.778A>T | XP_011531177.1:p.Met260Leu | |
XM_011532876.2:c.778A>T | XP_011531178.1:p.Met260Leu | |
NM_015717.5:c.778A>T MANE Select | NP_056532.4:p.Met260Leu |