Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33650279C= , CM000668.2:g.33650279C= | GRCh38 |
| NC_000006.11:g.33618056C= , CM000668.1:g.33618056C= | GRCh37 |
| NC_000006.10:g.33726034C= | NCBI36 |
| NG_027729.1:g.33901C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000605930.3:c.161-5487C= MANE Select | ENSP00000475177.1:n.161-5487C= | |
| ENST00000374316.9:c.161-5487C= | ENSP00000363435.4:n.161-5487C= | |
| ENST00000605930.2:c.161-5487C= | ENSP00000475177.1:n.161-5487C= | |
| NM_002224.3:c.161-5487C= | NP_002215.2:n.161-5487C= | |
| XM_011514576.1:c.230-5487C= | XP_011512878.1:n.230-5487C= | |
| XM_017010832.1:c.161-5487C= | XP_016866321.1:n.161-5487C= | |
| NM_002224.4:c.161-5487C= MANE Select | NP_002215.2:n.161-5487C= |