HGVS | Genome Assembly |
---|---|
NC_000020.11:g.59030336G= , CM000682.2:g.59030336G= | GRCh38 |
NC_000020.10:g.57605391G= , CM000682.1:g.57605391G= | GRCh37 |
NC_000020.9:g.57038786G= | NCBI36 |
NG_031871.1:g.7032C= | |
NG_031871.2:g.7032C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243997.8:c.126C= MANE Select | ENSP00000243997.3:p.Asn42= | |
ENST00000243997.7:c.126C= | ENSP00000243997.3:p.Asn42= | |
ENST00000395659.1:c.126C= | ENSP00000379019.1:p.Asn42= | |
ENST00000395663.1:c.126C= | ENSP00000379023.1:p.Asn42= | |
NM_006886.3:c.126C= | NP_008817.1:p.Asn42= | |
NR_037929.1:n.830C= | ||
NR_037930.1:n.571C= | ||
NM_006886.4:c.126C= MANE Select | NP_008817.1:p.Asn42= |