Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19965319G= , CM000670.2:g.19965319G= | GRCh38 |
| NC_000008.10:g.19822830G= , CM000670.1:g.19822830G= | GRCh37 |
| NC_000008.9:g.19867110G= | NCBI36 |
| NG_008855.1:g.31249G= | |
| NG_008855.2:g.68603G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.*9G= MANE Select | NP_000228.1:n.*9G= |
| ENST00000650287.1:c.*9G= MANE Select | ENSP00000497642.1:n.*9G= |
| NM_000237.2:c.*9G= | NP_000228.1:n.*9G= |
| ENST00000311322.8:c.*9G= | ENSP00000309757.6:n.*9G= |
| ENST00000650478.1:c.377G= | ENSP00000497560.1:n.377G= |