Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101615721C= , CM000671.2:g.101615721C= | GRCh38 |
| NC_000009.11:g.104378003C= , CM000671.1:g.104378003C= | GRCh37 |
| NC_000009.10:g.103417824C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_133445.3:c.2615-2194G= MANE Select | NP_597702.2:n.2615-2194G= |
| ENST00000361820.6:c.2615-2194G= MANE Select | ENSP00000355155.3:n.2615-2194G= |
| NM_133445.2:c.2615-2194G= | NP_597702.2:n.2615-2194G= |
| ENST00000361820.3:c.2615-2194G= | ENSP00000355155.3:n.2615-2194G= |
| XM_011518211.1:c.2615-2194G= | XP_011516513.1:n.2615-2194G= |
| XM_011518211.2:c.2615-2194G= | XP_011516513.1:n.2615-2194G= |
| XM_011518212.1:c.2615-2194G= | XP_011516514.1:n.2615-2194G= |
| XR_929711.1:n.2702-2194G= |