Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60648861C= , CM000676.2:g.60648861C= | GRCh38 |
| NC_000014.8:g.61115579C= , CM000676.1:g.61115579C= | GRCh37 |
| NC_000014.7:g.60185332C= | NCBI36 |
| NG_008231.1:g.5577G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005982.4:c.329G= MANE Select | NP_005973.1:p.Arg110= |
| ENST00000645694.3:c.329G= MANE Select | ENSP00000494686.1:p.Arg110= |
| NM_005982.3:c.329G= | NP_005973.1:p.Arg110= |
| ENST00000247182.6:c.329G= | ENSP00000247182.5:p.Arg110= |
| ENST00000553535.2:n.249-2284G= | |
| ENST00000554986.2:c.42-2284G= | ENSP00000452700.2:n.42-2284G= |
| ENST00000555955.3:n.1198-2284G= | |
| XM_017021602.2:c.329G= | XP_016877091.1:p.Arg110= |