Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204165389A>G , CM000663.2:g.204165389A>G | GRCh38 |
| NC_000001.10:g.204134517A>G , CM000663.1:g.204134517A>G | GRCh37 |
| NC_000001.9:g.202401140A>G | NCBI36 |
| NG_012122.1:g.5949T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.98+807T>C MANE Select | ENSP00000272190.8:n.98+807T>C | |
| ENST00000638118.1:c.-16-3226T>C | ENSP00000490307.1:n.-16-3226T>C | |
| ENST00000272190.8:c.98+807T>C | ENSP00000272190.8:n.98+807T>C | |
| NM_000537.3:c.98+807T>C | NP_000528.1:n.98+807T>C | |
| NM_000537.4:c.98+807T>C MANE Select | NP_000528.1:n.98+807T>C |