Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.70579486A= , CM000668.2:g.70579486A= | GRCh38 |
| NC_000006.11:g.71289189A= , CM000668.1:g.71289189A= | GRCh37 |
| NC_000006.10:g.71345910A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_145267.3:c.137A= MANE Select | NP_660310.2:p.Gln46= |
| ENST00000370474.4:c.137A= MANE Select | ENSP00000359505.3:p.Gln46= |
| NM_145267.2:c.137A= | NP_660310.2:p.Gln46= |
| ENST00000370474.3:c.137A= | ENSP00000359505.3:p.Gln46= |