Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.1649039T= , CM000664.2:g.1649039T= | GRCh38 |
| NC_000002.11:g.1652811T= , CM000664.1:g.1652811T= | GRCh37 |
| NC_000002.10:g.1631818T= | NCBI36 |
| NG_034221.1:g.100509A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012293.3:c.2741A= MANE Select | NP_036425.1:p.Asn914= |
| ENST00000252804.9:c.2741A= MANE Select | ENSP00000252804.4:p.Asn914= |
| NM_012293.2:c.2741A= | NP_036425.1:p.Asn914= |
| ENST00000252804.8:c.2741A= | ENSP00000252804.4:p.Asn914= |
| ENST00000478155.5:n.2697-4287A= | |
| XM_005264707.2:c.2669A= | XP_005264764.1:p.Asn890= |
| XM_005264707.3:c.2669A= | XP_005264764.1:p.Asn890= |
| XM_011510395.1:c.2552A= | XP_011508697.1:p.Asn851= |
| XM_011510396.1:c.2192A= | XP_011508698.1:p.Asn731= |
| XM_011510397.1:c.2192A= | XP_011508699.1:p.Asn731= |