HGVS | Genome Assembly |
---|---|
NC_000008.11:g.95260444T>A , CM000670.2:g.95260444T>A | GRCh38 |
NC_000008.10:g.96272672T>A , CM000670.1:g.96272672T>A | GRCh37 |
NC_000008.9:g.96341848T>A | NCBI36 |
NG_032804.1:g.13791A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286688.6:c.308+24A>T MANE Select | ENSP00000286688.5:n.308+24A>T | |
ENST00000286688.5:c.308+24A>T | ENSP00000286688.5:n.308+24A>T | |
NM_177965.3:c.308+24A>T | NP_808880.1:n.308+24A>T | |
XM_005250799.2:c.647+24A>T | XP_005250856.2:n.647+24A>T | |
NM_001363260.1:c.308+24A>T | NP_001350189.1:n.308+24A>T | |
NM_177965.4:c.308+24A>T MANE Select | NP_808880.1:n.308+24A>T |