Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31576050G>T , CM000668.2:g.31576050G>T | GRCh38 |
| NC_000006.11:g.31543827G>T , CM000668.1:g.31543827G>T | GRCh37 |
| NC_000006.10:g.31651806G>T | NCBI36 |
| NG_007462.1:g.5478G>T | |
| NG_012010.1:g.8952G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000594.4:c.186+123G>T MANE Select | NP_000585.2:n.186+123G>T |
| ENST00000449264.3:c.186+123G>T MANE Select | ENSP00000398698.2:n.186+123G>T |
| NM_000594.3:c.186+123G>T | NP_000585.2:n.186+123G>T |
| ENST00000449264.2:c.186+123G>T | ENSP00000398698.2:n.186+123G>T |
| ENST00000699334.1:c.186+123G>T | ENSP00000514308.1:n.186+123G>T |