Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48520878T>A , CM000677.2:g.48520878T>A | GRCh38 |
| NC_000015.9:g.48813075T>A , CM000677.1:g.48813075T>A | GRCh37 |
| NC_000015.8:g.46600367T>A | NCBI36 |
| NG_008805.2:g.129911A>T , LRG_778:g.129911A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.989-61A>T | ENSP00000453958.2:n.989-61A>T | |
| ENST00000674301.2:c.989-61A>T | ENSP00000501333.2:n.989-61A>T | |
| ENST00000316623.10:c.989-61A>T MANE Select | ENSP00000325527.5:n.989-61A>T | |
| ENST00000316623.9:c.989-61A>T | ENSP00000325527.5:n.989-61A>T | |
| ENST00000537463.6:c.636+16833A>T | ENSP00000440294.2:n.636+16833A>T | |
| NM_000138.4:c.989-61A>T , LRG_778t1:c.989-61A>T | NP_000129.3:n.989-61A>T | |
| NM_000138.5:c.989-61A>T MANE Select | NP_000129.3:n.989-61A>T |