Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135031028T= , CM000667.2:g.135031028T= | GRCh38 |
| NC_000005.9:g.134366718T= , CM000667.1:g.134366718T= | GRCh37 |
| NC_000005.8:g.134394617T= | NCBI36 |
| NG_012114.1:g.8247A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.402+248A= MANE Select | ENSP00000265340.6:n.402+248A= | |
| ENST00000265340.11:c.402+248A= | ENSP00000265340.6:n.402+248A= | |
| ENST00000503586.1:c.524+248A= | ||
| ENST00000504936.1:n.735+248A= | ||
| ENST00000506438.5:c.402+248A= | ENSP00000427542.1:n.402+248A= | |
| NM_002653.4:c.402+248A= | NP_002644.4:n.402+248A= | |
| NM_002653.5:c.402+248A= MANE Select | NP_002644.4:n.402+248A= |