HGVS | Genome Assembly |
---|---|
NC_000008.11:g.64624492C= , CM000670.2:g.64624492C= | GRCh38 |
NC_000008.10:g.65537049C= , CM000670.1:g.65537049C= | GRCh37 |
NC_000008.9:g.65699603C= | NCBI36 |
NG_008338.1:g.179300G= | |
NG_008338.2:g.179300G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000310193.4:c.170G= MANE Select | ENSP00000310721.3:p.Gly57= | |
ENST00000310193.3:c.170G= | ENSP00000310721.3:p.Gly57= | |
NM_004820.3:c.170G= | NP_004811.1:p.Gly57= | |
NM_001324112.1:c.170G= | NP_001311041.1:p.Gly57= | |
NM_004820.4:c.170G= | NP_004811.1:p.Gly57= | |
XM_017014002.1:c.236G= | XP_016869491.1:p.Gly79= | |
NM_004820.5:c.170G= MANE Select | NP_004811.1:p.Gly57= | |
NM_001324112.2:c.170G= | NP_001311041.1:p.Gly57= |