Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52451657T= , CM000674.2:g.52451657T= | GRCh38 |
| NC_000012.11:g.52845441T= , CM000674.1:g.52845441T= | GRCh37 |
| NC_000012.10:g.51131708T= | NCBI36 |
| NG_008299.1:g.5470A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252252.4:c.422A= MANE Select | ENSP00000252252.3:p.Asn141= | |
| ENST00000252252.3:c.422A= | ENSP00000252252.3:p.Asn141= | |
| NM_005555.3:c.422A= | NP_005546.2:p.Asn141= | |
| NM_005555.4:c.422A= MANE Select | NP_005546.2:p.Asn141= |