Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912054A= , CM000674.2:g.4912054A= | GRCh38 |
| NC_000012.11:g.5021220A= , CM000674.1:g.5021220A= | GRCh37 |
| NC_000012.10:g.4891481A= | NCBI36 |
| NG_011815.1:g.7148A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000217.3:c.676A= MANE Select | NP_000208.2:p.Thr226= |
| ENST00000382545.5:c.676A= MANE Select | ENSP00000371985.3:p.Thr226= |
| NM_000217.2:c.676A= | NP_000208.2:p.Thr226= |
| ENST00000382545.3:c.676A= | ENSP00000371985.3:p.Thr226= |
| ENST00000541095.1:n.105+1582A= | |
| ENST00000543874.2:n.96+1582A= | |
| ENST00000543874.3:n.105+1582A= | |
| ENST00000639306.1:c.514A= | ENSP00000492506.1:p.Thr172= |