Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6087017C= , CM000674.2:g.6087017C= | GRCh38 |
| NC_000012.11:g.6196183C= , CM000674.1:g.6196183C= | GRCh37 |
| NC_000012.10:g.6066444C= | NCBI36 |
| NG_009072.1:g.42654G= | |
| NG_009072.2:g.42654G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.657+8443G= MANE Select | ENSP00000261405.5:n.657+8443G= | |
| ENST00000261405.9:c.657+8443G= | ENSP00000261405.5:n.657+8443G= | |
| ENST00000538635.5:n.420+23498G= | ||
| NM_000552.3:c.657+8443G= | NP_000543.2:n.657+8443G= | |
| NM_000552.4:c.657+8443G= | NP_000543.2:n.657+8443G= | |
| NM_000552.5:c.657+8443G= MANE Select | NP_000543.3:n.657+8443G= |