Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68444528C= , CM000663.2:g.68444528C= | GRCh38 |
| NC_000001.10:g.68910211C= , CM000663.1:g.68910211C= | GRCh37 |
| NC_000001.9:g.68682799C= | NCBI36 |
| NG_008472.1:g.10432G= | |
| NG_008472.2:g.10432G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.495+3G= MANE Select | ENSP00000262340.5:n.495+3G= | |
| ENST00000262340.5:c.495+3G= | ENSP00000262340.5:n.495+3G= | |
| NM_000329.2:c.495+3G= | NP_000320.1:n.495+3G= | |
| XM_017002027.1:c.219+3G= | XP_016857516.1:n.219+3G= | |
| NM_000329.3:c.495+3G= MANE Select | NP_000320.1:n.495+3G= |