Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100642673A= , CM000669.2:g.100642673A= | GRCh38 |
| NC_000007.13:g.100240296A= , CM000669.1:g.100240296A= | GRCh37 |
| NC_000007.12:g.100078232A= | NCBI36 |
| NG_007989.1:g.3878T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000462107.1:c.-258+18T= | ENSP00000420525.1:n.-258+18T= |
| ENST00000474947.1:n.89+18T= | |
| XM_005250553.3:c.-258+18T= | XP_005250610.1:n.-258+18T= |
| XM_005250553.4:c.-258+18T= | XP_005250610.1:n.-258+18T= |
| XM_005250554.3:c.-258+18T= | XP_005250611.1:n.-258+18T= |
| XM_017012573.1:c.-70+18T= | XP_016868062.1:n.-70+18T= |