Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928897G= , CM000684.2:g.43928897G= | GRCh38 |
| NC_000022.10:g.44324777G= , CM000684.1:g.44324777G= | GRCh37 |
| NC_000022.9:g.42656110G= | NCBI36 |
| NG_008631.1:g.10159G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.486+8G= MANE Select | ENSP00000216180.3:n.486+8G= | |
| ENST00000216180.7:c.486+8G= | ENSP00000216180.3:n.486+8G= | |
| ENST00000406117.6:c.*118+8G= | ENSP00000384668.2:n.*118+8G= | |
| ENST00000423180.2:c.474+8G= | ENSP00000397987.2:n.474+8G= | |
| ENST00000478713.1:n.520+8G= | ||
| NM_025225.2:c.486+8G= | NP_079501.2:n.486+8G= | |
| NM_025225.3:c.486+8G= MANE Select | NP_079501.2:n.486+8G= |