Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837238T= , CM000670.2:g.117837238T= | GRCh38 |
| NC_000008.10:g.118849477T= , CM000670.1:g.118849477T= | GRCh37 |
| NC_000008.9:g.118918658T= | NCBI36 |
| NG_007455.2:g.279582A= , LRG_493:g.279582A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.430-37A= | ||
| ENST00000378204.7:c.963-37A= MANE Select | ENSP00000367446.3:n.963-37A= | |
| ENST00000436216.2:c.331-37A= | ||
| ENST00000378204.6:c.963-37A= | ENSP00000367446.2:n.963-37A= | |
| ENST00000436216.1:c.331-37A= | ||
| ENST00000437196.1:c.74-1687A= | ENSP00000407299.1:n.74-1687A= | |
| NM_000127.2:c.963-37A= , LRG_493t1:c.963-37A= | NP_000118.2:n.963-37A= | |
| NM_000127.3:c.963-37A= MANE Select | NP_000118.2:n.963-37A= |