Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652674T= , CM000663.2:g.171652674T= | GRCh38 |
| NC_000001.10:g.171621814T= , CM000663.1:g.171621814T= | GRCh37 |
| NC_000001.9:g.169888437T= | NCBI36 |
| NG_008859.1:g.4960A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.-63A= MANE Select | ENSP00000037502.5:n.-63A= | |
| ENST00000037502.10:c.-63A= | ENSP00000037502.5:n.-63A= | |
| NM_000261.2:c.-63A= MANE Select | NP_000252.1:n.-63A= |