Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071730T>C , CM000667.2:g.111071730T>C | GRCh38 |
| NC_000005.9:g.110407428T>C , CM000667.1:g.110407428T>C | GRCh37 |
| NC_000005.8:g.110435327T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.-161T>C MANE Select | ENSP00000339804.3:n.-161T>C | |
| ENST00000344895.3:c.-161T>C | ENSP00000339804.3:n.-161T>C | |
| ENST00000420978.6:c.35-195T>C | ENSP00000399099.2:n.35-195T>C | |
| NM_033035.4:c.-161T>C | NP_149024.1:n.-161T>C | |
| NR_045089.1:n.1439-195T>C | ||
| NM_033035.5:c.-161T>C MANE Select | NP_149024.1:n.-161T>C | |
| NR_045089.2:n.1457-195T>C |