Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.113387783T= , CM000667.2:g.113387783T= | GRCh38 |
| NC_000005.9:g.112723480T= , CM000667.1:g.112723480T= | GRCh37 |
| NC_000005.8:g.112751379T= | NCBI36 |
| NG_012265.1:g.106048A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000408903.7:c.171-2571A= MANE Select | ENSP00000386227.3:n.171-2571A= | |
| ENST00000408903.6:c.171-2571A= | ENSP00000386227.3:n.171-2571A= | |
| NM_001085377.1:c.171-2571A= | NP_001078846.1:n.171-2571A= | |
| XM_017009473.1:c.171-2571A= | XP_016864962.1:n.171-2571A= | |
| NM_001085377.2:c.171-2571A= MANE Select | NP_001078846.2:n.171-2571A= |