Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.73640827A= , CM000664.2:g.73640827A= | GRCh38 |
| NC_000002.11:g.73867954A= , CM000664.1:g.73867954A= | GRCh37 |
| NC_000002.10:g.73721462A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272425.4:c.*118T= MANE Select | ENSP00000272425.3:n.*118T= | |
| NM_003960.3:c.*118T= | NP_003951.3:n.*118T= | |
| NM_003960.4:c.*118T= MANE Select | NP_003951.3:n.*118T= |