Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.27797676G>T , CM000679.2:g.27797676G>T | GRCh38 |
| NC_000017.10:g.26124702G>T , CM000679.1:g.26124702G>T | GRCh37 |
| NC_000017.9:g.23148829G>T | NCBI36 |
| NG_011470.1:g.7854C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000697337.1:c.110+1024C>A | ENSP00000513259.1:n.110+1024C>A | |
| ENST00000313735.11:c.110+1024C>A MANE Select | ENSP00000327251.6:n.110+1024C>A | |
| ENST00000313735.10:c.110+1024C>A | ENSP00000327251.6:n.110+1024C>A | |
| ENST00000621962.1:c.110+1024C>A | ENSP00000482291.1:n.110+1024C>A | |
| NM_000625.4:c.110+1024C>A MANE Select | NP_000616.3:n.110+1024C>A | |
| XM_011524859.1:c.110+1024C>A | XP_011523161.1:n.110+1024C>A | |
| XM_011524861.1:c.110+1024C>A | XP_011523163.1:n.110+1024C>A |