HGVS | Genome Assembly |
---|---|
NC_000007.14:g.27095685C= , CM000669.2:g.27095685C= | GRCh38 |
NC_000007.13:g.27135304C= , CM000669.1:g.27135304C= | GRCh37 |
NC_000007.12:g.27101829C= | NCBI36 |
NG_011813.1:g.5322G= | |
NG_033087.1:g.4592C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000643460.2:c.228G= MANE Select | ENSP00000494260.2:p.Gln76= | |
ENST00000343060.4:c.228G= | ENSP00000343246.4:p.Gln76= | |
ENST00000355633.5:c.228G= | ENSP00000347851.5:p.Gln76= | |
NM_005522.4:c.228G= | NP_005513.1:p.Gln76= | |
NM_153620.2:c.228G= | NP_705873.2:p.Gln76= | |
NM_005522.5:c.228G= MANE Select | NP_005513.2:p.Gln76= | |
NM_153620.3:c.228G= | NP_705873.3:p.Gln76= |