Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.132477995A= , CM000665.2:g.132477995A= | GRCh38 |
| NC_000003.11:g.132196839A= , CM000665.1:g.132196839A= | GRCh37 |
| NC_000003.10:g.133679529A= | NCBI36 |
| NG_051045.1:g.65469A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260818.11:c.2564A= MANE Select | ENSP00000260818.6:p.Asn855= | |
| ENST00000650455.1:c.*712A= | ENSP00000496825.1:n.*712A= | |
| ENST00000260818.10:c.2564A= | ENSP00000260818.6:p.Asn855= | |
| ENST00000464766.1:n.401A= | ||
| NM_015268.3:c.2564A= | NP_056083.3:p.Asn855= | |
| XM_005247245.3:c.2579A= | XP_005247302.1:p.Asn860= | |
| NM_001329126.1:c.2579A= | NP_001316055.1:p.Asn860= | |
| XM_017006036.1:c.533A= | XP_016861525.1:p.Asn178= | |
| NM_015268.4:c.2564A= MANE Select | NP_056083.3:p.Asn855= | |
| NM_001329126.2:c.2579A= | NP_001316055.1:p.Asn860= |