Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118308416T>C , CM000673.2:g.118308416T>C | GRCh38 |
| NC_000011.9:g.118179131T>C , CM000673.1:g.118179131T>C | GRCh37 |
| NC_000011.8:g.117684341T>C | NCBI36 |
| NG_007383.1:g.8837T>C , LRG_38:g.8837T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000733.4:c.71-11T>C MANE Select | NP_000724.1:n.71-11T>C |
| ENST00000361763.9:c.71-11T>C MANE Select | ENSP00000354566.4:n.71-11T>C |
| NM_000733.3:c.71-11T>C , LRG_38t1:c.71-11T>C | NP_000724.1:n.71-11T>C |
| ENST00000361763.8:c.71-11T>C | ENSP00000354566.4:n.71-11T>C |
| ENST00000526146.5:n.170-11T>C | |
| ENST00000528435.5:n.177-11T>C | |
| ENST00000528600.1:c.71-11T>C | ENSP00000433975.1:n.71-11T>C |
| ENST00000529713.5:n.177-11T>C |