Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.106285307C= , CM000669.2:g.106285307C= | GRCh38 |
| NC_000007.13:g.105925753C= , CM000669.1:g.105925753C= | GRCh37 |
| NC_000007.12:g.105712989C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000417537.1:c.-48+234G= | ENSP00000390896.1:n.-48+234G= |
| ENST00000424768.1:c.-98+234G= | ENSP00000390591.1:n.-98+234G= |
| ENST00000424768.2:c.-98+234G= | ENSP00000390591.2:n.-98+234G= |
| ENST00000681255.1:c.-48+234G= | ENSP00000506129.1:n.-48+234G= |
| ENST00000681491.1:c.-98+11G= | ENSP00000506540.1:n.-98+11G= |
| XM_005250100.1:c.-98+234G= | XP_005250157.1:n.-98+234G= |