Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.38696786A>G , CM000668.2:g.38696786A>G | GRCh38 |
| NC_000006.11:g.38664562A>G , CM000668.1:g.38664562A>G | GRCh37 |
| NC_000006.10:g.38772540A>G | NCBI36 |
| NG_012074.1:g.11391T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373365.5:c.84+6185T>C MANE Select | ENSP00000362463.3:n.84+6185T>C | |
| ENST00000373365.4:c.84+6185T>C | ENSP00000362463.3:n.84+6185T>C | |
| NM_006708.2:c.84+6185T>C | NP_006699.2:n.84+6185T>C | |
| NM_006708.3:c.84+6185T>C MANE Select | NP_006699.2:n.84+6185T>C |