HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47733460C>A , CM000679.2:g.47733460C>A | GRCh38 |
NC_000017.10:g.45810826C>A , CM000679.1:g.45810826C>A | GRCh37 |
NC_000017.9:g.43165825C>A | NCBI36 |
NG_012166.1:g.5217C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000177694.2:c.6C>A MANE Select | ENSP00000177694.1:p.Gly2= | |
ENST00000177694.1:c.6C>A | ENSP00000177694.1:p.Gly2= | |
ENST00000581328.1:n.36C>A | ||
NM_013351.1:c.6C>A | NP_037483.1:p.Gly2= | |
XM_011524698.1:c.6C>A | XP_011523000.1:p.Gly2= | |
NM_013351.2:c.6C>A MANE Select | NP_037483.1:p.Gly2= |