Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190404955G= , CM000665.2:g.190404955G= | GRCh38 |
| NC_000003.11:g.190122744G= , CM000665.1:g.190122744G= | GRCh37 |
| NC_000003.10:g.191605438G= | NCBI36 |
| NG_008149.1:g.21904G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.382+29G= MANE Select | ENSP00000264734.3:n.382+29G= | |
| ENST00000456423.2:c.115-4948G= | ENSP00000414136.2:n.115-4948G= | |
| ENST00000264734.2:c.592+29G= | ENSP00000264734.2:n.592+29G= | |
| ENST00000456423.1:c.325-4948G= | ENSP00000414136.1:n.325-4948G= | |
| NM_006580.3:c.592+29G= | NP_006571.1:n.592+29G= | |
| NM_001378492.1:c.382+29G= | NP_001365421.1:n.382+29G= | |
| NM_001378493.1:c.382+29G= | NP_001365422.1:n.382+29G= | |
| NM_006580.4:c.382+29G= MANE Select | NP_006571.2:n.382+29G= |