Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40931905G= , CM000677.2:g.40931905G= | GRCh38 |
| NC_000015.9:g.41224103G= , CM000677.1:g.41224103G= | GRCh37 |
| NC_000015.8:g.39011395G= | NCBI36 |
| NG_046974.1:g.7573G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249749.7:c.658+139G= MANE Select | ENSP00000249749.5:n.658+139G= | |
| ENST00000249749.6:c.658+139G= | ENSP00000249749.5:n.658+139G= | |
| ENST00000559440.1:n.887+139G= | ||
| NM_019074.3:c.658+139G= | NP_061947.1:n.658+139G= | |
| NM_019074.4:c.658+139G= MANE Select | NP_061947.1:n.658+139G= |