Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33055634T>A , CM000675.2:g.33055634T>A | GRCh38 |
| NC_000013.10:g.33629771T>A , CM000675.1:g.33629771T>A | GRCh37 |
| NC_000013.9:g.32527771T>A | NCBI36 |
| NG_011485.1:g.44201T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380099.4:c.1599+319T>A MANE Select | ENSP00000369442.3:n.1599+319T>A | |
| ENST00000380099.3:c.1599+319T>A | ENSP00000369442.3:n.1599+319T>A | |
| ENST00000487852.1:n.1657+269T>A | ||
| NM_004795.3:c.1599+319T>A | NP_004786.2:n.1599+319T>A | |
| XM_006719895.1:c.678+319T>A | XP_006719958.1:n.678+319T>A | |
| XM_006719895.2:c.678+319T>A | XP_006719958.1:n.678+319T>A | |
| NM_004795.4:c.1599+319T>A MANE Select | NP_004786.2:n.1599+319T>A |