Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89721313A= , CM000666.2:g.89721313A= | GRCh38 |
| NC_000004.11:g.90642464A= , CM000666.1:g.90642464A= | GRCh37 |
| NC_000004.10:g.90861487A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673902.1:c.390+7881T= | ENSP00000501102.1:n.390+7881T= | |
| XR_001741765.1:n.4196A= | ||
| XR_001741766.1:n.2968A= | ||
| XR_938982.2:n.4778A= | ||
| XR_938984.2:n.4200A= | ||
| XR_938985.2:n.3232A= | ||
| XR_938986.2:n.1869A= | ||
| XR_938987.2:n.2158A= | ||
| XR_938989.2:n.1642A= |