Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157109473C= , CM000667.2:g.157109473C= | GRCh38 |
| NC_000005.9:g.156536484C= , CM000667.1:g.156536484C= | GRCh37 |
| NC_000005.8:g.156469062C= | NCBI36 |
| NG_030444.1:g.4765G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524219.2:c.-293-2511G= | ENSP00000430328.2:n.-293-2511G= | |
| ENST00000696899.1:c.-264-226G= | ENSP00000512960.1:n.-264-226G= | |
| ENST00000696901.1:c.-490G= | ENSP00000512962.1:n.-490G= | |
| ENST00000307851.8:c.-490G= | ENSP00000312002.4:n.-490G= | |
| ENST00000524219.1:c.-293-2511G= | ENSP00000430328.1:n.-293-2511G= |