HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116748569A= , CM000673.2:g.116748569A= | GRCh38 |
NC_000011.9:g.116619285A= , CM000673.1:g.116619285A= | GRCh37 |
NC_000011.8:g.116124495A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260210.5:c.1773T= MANE Select | ENSP00000260210.3:p.Asn591= | |
ENST00000260210.4:c.1773T= | ENSP00000260210.3:p.Asn591= | |
ENST00000375445.7:c.1371T= | ENSP00000364594.3:p.Asn457= | |
ENST00000419189.1:c.548T= | ||
NM_001159736.1:c.1371T= | NP_001153208.1:p.Asn457= | |
NM_032725.3:c.1773T= | NP_116114.1:p.Asn591= | |
XM_011543035.1:c.1674T= | XP_011541337.1:p.Asn558= | |
XM_011543035.2:c.1674T= | XP_011541337.1:p.Asn558= | |
NM_032725.4:c.1773T= MANE Select | NP_116114.1:p.Asn591= | |
NM_001159736.2:c.1371T= | NP_001153208.1:p.Asn457= |