Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149576460G= , CM000664.2:g.149576460G= | GRCh38 |
| NC_000002.11:g.150432974G= , CM000664.1:g.150432974G= | GRCh37 |
| NC_000002.10:g.150141220G= | NCBI36 |
| NG_009189.1:g.16357C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_015702.3:c.455C= MANE Select | NP_056517.1:p.Thr152= |
| ENST00000303319.10:c.455C= MANE Select | ENSP00000301920.5:p.Thr152= |
| NM_015702.2:c.455C= | NP_056517.1:p.Thr152= |
| ENST00000303319.9:c.455C= | ENSP00000301920.5:p.Thr152= |
| ENST00000422782.2:c.455C= | ENSP00000408331.2:p.Thr152= |
| ENST00000428879.5:c.455C= | ENSP00000389060.1:p.Thr152= |