Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.77586643T= , CM000666.2:g.77586643T= | GRCh38 |
| NC_000004.11:g.78507797T= , CM000666.1:g.78507797T= | GRCh37 |
| NC_000004.10:g.78726821T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286758.4:c.-42-19181T= | ENSP00000286758.4:n.-42-19181T= | |
| NM_006419.2:c.-42-19181T= | NP_006410.1:n.-42-19181T= | |
| XR_938912.1:n.1013A= | ||
| XR_938913.1:n.930+1058A= | ||
| XR_001741743.1:n.1605A= | ||
| XR_938912.2:n.1889A= | ||
| NM_006419.3:c.-42-19181T= | NP_006410.1:n.-42-19181T= |