Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7533947G= , CM000681.2:g.7533947G= | GRCh38 |
| NC_000019.9:g.7598833G= , CM000681.1:g.7598833G= | GRCh37 |
| NC_000019.8:g.7504833G= | NCBI36 |
| NG_013374.1:g.4796G= | |
| NG_015806.1:g.16338G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.*152G= MANE Select | ENSP00000264079.5:n.*152G= | |
| ENST00000264079.10:c.*152G= | ENSP00000264079.5:n.*152G= | |
| ENST00000394321.9:n.2210G= | ||
| ENST00000599334.1:c.623G= | ||
| ENST00000601870.1:c.169+79G= | ||
| ENST00000602227.1:n.449G= | ||
| NM_020533.2:c.*152G= | NP_065394.1:n.*152G= | |
| NM_020533.3:c.*152G= MANE Select | NP_065394.1:n.*152G= |