dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.11254001T>G , CM000678.2:g.11254001T>G | GRCh38 |
| NC_000016.9:g.11347858T>G , CM000678.1:g.11347858T>G | GRCh37 |
| NC_000016.8:g.11255359T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649869.1:n.152+4223T>G | ||
| ENST00000572173.1:c.-516+4223T>G | ENSP00000461206.1:n.-516+4223T>G | |
| ENST00000573910.1:n.160+4223T>G | ||
| XR_933070.1:n.733+4223T>G | ||
| XR_933070.3:n.876+4223T>G |