HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160882111C>T , CM000663.2:g.160882111C>T | GRCh38 |
NC_000001.10:g.160851901C>T , CM000663.1:g.160851901C>T | GRCh37 |
NC_000001.9:g.159118525C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.251G>A MANE Select | ENSP00000323587.3:p.Ser84Asn | |
ENST00000326245.3:c.251G>A | ENSP00000323587.3:p.Ser84Asn | |
ENST00000464077.1:n.185G>A | ||
NM_017625.2:c.251G>A | NP_060095.2:p.Ser84Asn | |
NM_017625.3:c.251G>A MANE Select | NP_060095.2:p.Ser84Asn |