Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5969204G>A , CM000674.2:g.5969204G>A | GRCh38 |
| NC_000012.11:g.6078370G>A , CM000674.1:g.6078370G>A | GRCh37 |
| NC_000012.10:g.5948631G>A | NCBI36 |
| NG_009072.1:g.160467C>T | |
| NG_009072.2:g.160467C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000552.5:c.7729+7C>T MANE Select | NP_000543.3:n.7729+7C>T |
| ENST00000261405.10:c.7729+7C>T MANE Select | ENSP00000261405.5:n.7729+7C>T |
| NM_000552.3:c.7729+7C>T | NP_000543.2:n.7729+7C>T |
| NM_000552.4:c.7729+7C>T | NP_000543.2:n.7729+7C>T |
| ENST00000261405.9:c.7729+7C>T | ENSP00000261405.5:n.7729+7C>T |