Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218882172A>T , CM000664.2:g.218882172A>T | GRCh38 |
| NC_000002.11:g.219746894A>T , CM000664.1:g.219746894A>T | GRCh37 |
| NC_000002.10:g.219455138A>T | NCBI36 |
| NG_012179.1:g.6640A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.125A>T MANE Select | ENSP00000258411.3:p.Asn42Ile | |
| ENST00000258411.7:c.125A>T | ENSP00000258411.3:p.Asn42Ile | |
| ENST00000458582.1:c.12A>T | ||
| NM_025216.2:c.125A>T | NP_079492.2:p.Asn42Ile | |
| XM_011511928.1:c.74A>T | XP_011510230.1:p.Asn25Ile | |
| XM_011511929.1:c.29A>T | XP_011510231.1:p.Asn10Ile | |
| XM_011511930.1:c.125A>T | XP_011510232.1:p.Asn42Ile | |
| XM_011511929.2:c.29A>T | XP_011510231.1:p.Asn10Ile | |
| NM_025216.3:c.125A>T MANE Select | NP_079492.2:p.Asn42Ile |