Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.8501632A>T , CM000666.2:g.8501632A>T | GRCh38 |
| NC_000004.11:g.8503359A>T , CM000666.1:g.8503359A>T | GRCh37 |
| NC_000004.10:g.8554259A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_006713862.2:c.2045-7166A>T | XP_006713925.1:n.2045-7166A>T | |
| XR_427468.2:n.2086-7166A>T | ||
| XR_924914.1:n.2086-7166A>T | ||
| XR_924915.1:n.2086-7166A>T | ||
| XR_924916.1:n.2086-7166A>T | ||
| XR_001741149.1:n.2091-7166A>T | ||
| XR_001741150.2:n.2232-7166A>T | ||
| XR_427468.3:n.2091-7166A>T | ||
| XR_924916.2:n.2091-7166A>T |