Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.132091140C= , CM000670.2:g.132091140C= | GRCh38 |
| NC_000008.10:g.133103387C= , CM000670.1:g.133103387C= | GRCh37 |
| NC_000008.9:g.133172569C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000414222.2:c.449-1541G= MANE Select | ENSP00000388322.1:n.449-1541G= | |
| ENST00000673615.1:c.557-1541G= | ENSP00000500443.1:n.557-1541G= | |
| ENST00000414222.1:c.449-1541G= | ENSP00000388322.1:n.449-1541G= | |
| ENST00000434736.6:c.557-1541G= | ENSP00000407107.2:n.557-1541G= | |
| NM_001145095.1:c.449-1541G= | NP_001138567.1:n.449-1541G= | |
| NM_001145095.3:c.449-1541G= MANE Select | NP_001138567.1:n.449-1541G= |