Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.153071533G= , CM000663.2:g.153071533G= | GRCh38 |
| NC_000001.10:g.153044009G= , CM000663.1:g.153044009G= | GRCh37 |
| NC_000001.9:g.151310633G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368755.3:c.-20+36C= MANE Select | ENSP00000357744.1:n.-20+36C= | |
| NM_001017418.2:c.-20+32C= | NP_001017418.1:n.-20+32C= | |
| XM_017002174.1:c.-20+36C= | XP_016857663.1:n.-20+36C= | |
| NM_001017418.3:c.-20+32C= | NP_001017418.1:n.-20+32C= | |
| NM_001388198.1:c.-20+36C= MANE Select | NP_001375127.1:n.-20+36C= |