Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24658538T= , CM000668.2:g.24658538T= | GRCh38 |
| NC_000006.11:g.24658766T= , CM000668.1:g.24658766T= | GRCh37 |
| NC_000006.10:g.24766745T= | NCBI36 |
| NG_052787.1:g.13350A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378198.9:c.425+23A= MANE Select | ENSP00000367440.4:n.425+23A= | |
| ENST00000341060.3:c.251+23A= | ENSP00000345345.3:n.251+23A= | |
| ENST00000378198.8:c.425+23A= | ENSP00000367440.4:n.425+23A= | |
| ENST00000478285.1:n.612+23A= | ||
| ENST00000478507.1:n.320-5385A= | ||
| NM_016614.2:c.425+23A= | NP_057698.2:n.425+23A= | |
| XR_926244.1:n.552+23A= | ||
| NM_016614.3:c.425+23A= MANE Select | NP_057698.2:n.425+23A= |