Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.52316377G>A , CM000676.2:g.52316377G>A | GRCh38 |
| NC_000014.8:g.52783095G>A , CM000676.1:g.52783095G>A | GRCh37 |
| NC_000014.7:g.51852845G>A | NCBI36 |
| NG_013082.1:g.7080G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000956.4:c.843+986G>A MANE Select | NP_000947.2:n.843+986G>A |
| ENST00000245457.6:c.843+986G>A MANE Select | ENSP00000245457.5:n.843+986G>A |
| NM_000956.3:c.843+986G>A | NP_000947.2:n.843+986G>A |
| ENST00000245457.5:c.843+986G>A | ENSP00000245457.5:n.843+986G>A |
| ENST00000557436.1:c.78+986G>A | ENSP00000450933.1:n.78+986G>A |