Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1609955G= , CM000668.2:g.1609955G= | GRCh38 |
| NC_000006.11:g.1610190G= , CM000668.1:g.1610190G= | GRCh37 |
| NC_000006.10:g.1555189G= | NCBI36 |
| NG_009368.1:g.4510G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.-491G= MANE Select | ENSP00000493906.1:n.-491G= | |
| NM_001453.3:c.-491G= MANE Select | NP_001444.2:n.-491G= |