Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112226395G= , CM000673.2:g.112226395G= | GRCh38 |
| NC_000011.9:g.112097118G= , CM000673.1:g.112097118G= | GRCh37 |
| NC_000011.8:g.111602328G= | NCBI36 |
| NG_008743.1:g.5031G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000280362.7:c.-49G= | ENSP00000280362.3:n.-49G= | |
| ENST00000525645.1:n.27G= | ||
| ENST00000528679.5:c.-49G= | ENSP00000435895.1:n.-49G= | |
| ENST00000531673.5:c.-49G= | ENSP00000433469.1:n.-49G= | |
| NM_000317.2:c.-49G= | NP_000308.1:n.-49G= |