Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7526982T>G , CM000681.2:g.7526982T>G | GRCh38 |
| NC_000019.9:g.7591868T>G , CM000681.1:g.7591868T>G | GRCh37 |
| NC_000019.8:g.7497868T>G | NCBI36 |
| NG_015806.1:g.9373T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.571+56T>G MANE Select | ENSP00000264079.5:n.571+56T>G | |
| ENST00000264079.10:c.571+56T>G | ENSP00000264079.5:n.571+56T>G | |
| ENST00000394321.9:n.651+56T>G | ||
| ENST00000596008.1:n.589T>G | ||
| ENST00000598406.1:n.392+56T>G | ||
| ENST00000601003.1:c.571+56T>G | ENSP00000469074.1:n.571+56T>G | |
| NM_020533.2:c.571+56T>G | NP_065394.1:n.571+56T>G | |
| NM_020533.3:c.571+56T>G MANE Select | NP_065394.1:n.571+56T>G |