Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186208943G= , CM000666.2:g.186208943G= | GRCh38 |
| NC_000004.11:g.187130097G= , CM000666.1:g.187130097G= | GRCh37 |
| NC_000004.10:g.187367091G= | NCBI36 |
| NG_007965.1:g.22424G= | |
| NG_012095.2:g.4965G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378802.5:c.1169G= MANE Select | ENSP00000368079.4:p.Arg390= | |
| ENST00000378802.4:c.1169G= | ENSP00000368079.4:p.Arg390= | |
| ENST00000502665.1:n.404G= | ||
| ENST00000507209.5:n.5867G= | ||
| ENST00000513354.5:n.259G= | ||
| NM_207352.3:c.1169G= | NP_997235.3:p.Arg390= | |
| XM_005262935.2:c.1169G= | XP_005262992.1:p.Arg390= | |
| XM_006714184.2:c.773G= | XP_006714247.1:p.Arg258= | |
| XM_005262935.4:c.1169G= | XP_005262992.1:p.Arg390= | |
| XM_017008037.1:c.773G= | XP_016863526.1:p.Arg258= | |
| NM_207352.4:c.1169G= MANE Select | NP_997235.3:p.Arg390= |