Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.46412808C>A , CM000681.2:g.46412808C>A | GRCh38 |
| NC_000019.9:g.46916065C>A , CM000681.1:g.46916065C>A | GRCh37 |
| NC_000019.8:g.51607905C>A | NCBI36 |
| NG_031956.1:g.5855G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032040.5:c.3G>T MANE Select | NP_114429.2:p.Met1Ile |
| ENST00000307522.5:c.3G>T MANE Select | ENSP00000303158.3:p.Met1Ile |
| NM_032040.4:c.3G>T | NP_114429.2:p.Met1Ile |
| ENST00000307522.3:c.3G>T | ENSP00000303158.3:p.Met1Ile |
| ENST00000697726.1:c.213G>T | ENSP00000513420.1:p.Met71Ile |