Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.15174922C= , CM000665.2:g.15174922C= | GRCh38 |
| NC_000003.11:g.15216429C= , CM000665.1:g.15216429C= | GRCh37 |
| NC_000003.10:g.15191433C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000446690.2:n.1282G= | ||
| ENST00000487147.5:n.1106G= | ||
| ENST00000491915.1:n.182G= | ||
| NR_027927.1:n.1282G= |