HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86633112T>A , CM000670.2:g.86633112T>A | GRCh38 |
NC_000008.10:g.87645340T>A , CM000670.1:g.87645340T>A | GRCh37 |
NC_000008.9:g.87714456T>A | NCBI36 |
NG_016980.1:g.115564A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.1179-219A>T MANE Select | ENSP00000316605.5:n.1179-219A>T | |
ENST00000681546.1:n.999-219A>T | ||
ENST00000681746.1:c.1179-219A>T | ENSP00000505959.1:n.1179-219A>T | |
ENST00000320005.5:c.1179-219A>T | ENSP00000316605.5:n.1179-219A>T | |
NM_019098.4:c.1179-219A>T | NP_061971.3:n.1179-219A>T | |
XM_011517138.1:c.765-219A>T | XP_011515440.1:n.765-219A>T | |
XM_011517138.2:c.765-219A>T | XP_011515440.1:n.765-219A>T | |
NM_019098.5:c.1179-219A>T MANE Select | NP_061971.3:n.1179-219A>T |