Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215766665G>T , CM000663.2:g.215766665G>T | GRCh38 |
| NC_000001.10:g.215940007G>T , CM000663.1:g.215940007G>T | GRCh37 |
| NC_000001.9:g.214006630G>T | NCBI36 |
| NG_009497.1:g.661732C>A | |
| NG_009497.2:g.661784C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11047+16C>A MANE Select | ENSP00000305941.3:n.11047+16C>A | |
| ENST00000674083.1:c.11047+16C>A | ENSP00000501296.1:n.11047+16C>A | |
| ENST00000307340.7:c.11047+16C>A | ENSP00000305941.3:n.11047+16C>A | |
| NM_206933.2:c.11047+16C>A | NP_996816.2:n.11047+16C>A | |
| NM_206933.3:c.11047+16C>A | NP_996816.2:n.11047+16C>A | |
| NM_206933.4:c.11047+16C>A MANE Select | NP_996816.3:n.11047+16C>A |