Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216418693C= , CM000663.2:g.216418693C= | GRCh38 |
| NC_000001.10:g.216592035C= , CM000663.1:g.216592035C= | GRCh37 |
| NC_000001.9:g.214658658C= | NCBI36 |
| NG_009497.1:g.9704G= | |
| NG_009497.2:g.9756G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307340.8:c.486-14G= MANE Select | ENSP00000305941.3:n.486-14G= | |
| ENST00000674083.1:c.486-14G= | ENSP00000501296.1:n.486-14G= | |
| ENST00000307340.7:c.486-14G= | ENSP00000305941.3:n.486-14G= | |
| ENST00000366942.3:c.486-14G= | ENSP00000355909.3:n.486-14G= | |
| NM_007123.5:c.486-14G= | NP_009054.5:n.486-14G= | |
| NM_206933.2:c.486-14G= | NP_996816.2:n.486-14G= | |
| NM_206933.3:c.486-14G= | NP_996816.2:n.486-14G= | |
| NM_007123.6:c.486-14G= | NP_009054.6:n.486-14G= | |
| NM_206933.4:c.486-14G= MANE Select | NP_996816.3:n.486-14G= |