Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160650438G= , CM000668.2:g.160650438G= | GRCh38 |
| NC_000006.11:g.161071470G= , CM000668.1:g.161071470G= | GRCh37 |
| NC_000006.10:g.160991460G= | NCBI36 |
| NG_016147.1:g.20938C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005577.4:c.109C= MANE Select | NP_005568.2:p.Arg37= |
| ENST00000316300.10:c.109C= MANE Select | ENSP00000321334.6:p.Arg37= |
| NM_005577.2:c.109C= | NP_005568.2:p.Arg37= |
| NM_005577.3:c.109C= | NP_005568.2:p.Arg37= |
| ENST00000316300.9:c.109C= | ENSP00000321334.5:p.Arg37= |