Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8533079C>A , CM000685.2:g.8533079C>A | GRCh38 |
| NC_000023.10:g.8501120C>A , CM000685.1:g.8501120C>A | GRCh37 |
| NC_000023.9:g.8461120C>A | NCBI36 |
| NG_007088.1:g.204108G>T | |
| NG_007088.2:g.204108G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000216.4:c.1985-26G>T MANE Select | NP_000207.2:n.1985-26G>T |
| ENST00000262648.8:c.1985-26G>T MANE Select | ENSP00000262648.3:n.1985-26G>T |
| NM_000216.2:c.1985-26G>T | NP_000207.2:n.1985-26G>T |
| NM_000216.3:c.1985-26G>T | NP_000207.2:n.1985-26G>T |
| ENST00000262648.7:c.1985-26G>T | ENSP00000262648.3:n.1985-26G>T |
| ENST00000619786.1:c.1982-26G>T | ENSP00000478734.1:n.1982-26G>T |