HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94043476C>A , CM000663.2:g.94043476C>A | GRCh38 |
NC_000001.10:g.94509032C>A , CM000663.1:g.94509032C>A | GRCh37 |
NC_000001.9:g.94281620C>A | NCBI36 |
NG_009073.1:g.82674G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.3051-1G>T MANE Select | ENSP00000359245.3:n.3051-1G>T | |
ENST00000370225.3:c.3051-1G>T | ENSP00000359245.3:n.3051-1G>T | |
ENST00000536513.5:c.-64-3387G>T | ENSP00000439707.2:n.-64-3387G>T | |
NM_000350.2:c.3051-1G>T | NP_000341.2:n.3051-1G>T | |
NM_000350.3:c.3051-1G>T MANE Select | NP_000341.2:n.3051-1G>T |