HGVS | Genome Assembly |
---|---|
NC_000011.10:g.55811878T>C , CM000673.2:g.55811878T>C | GRCh38 |
NC_000011.9:g.55579354T>C , CM000673.1:g.55579354T>C | GRCh37 |
NC_000011.8:g.55335930T>C | NCBI36 |
NG_052620.1:g.5512T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000625203.2:c.412T>C MANE Select | ENSP00000485319.1:p.Trp138Arg | |
ENST00000333973.3:c.412T>C | ENSP00000335529.2:p.Trp138Arg | |
ENST00000623450.1:c.412T>C | ENSP00000485509.1:p.Trp138Arg | |
ENST00000625203.1:c.412T>C | ENSP00000485319.1:p.Trp138Arg | |
NM_001004738.1:c.412T>C | NP_001004738.1:p.Trp138Arg | |
NM_001004738.2:c.412T>C MANE Select | NP_001004738.1:p.Trp138Arg |