Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071719G= , CM000667.2:g.111071719G= | GRCh38 |
| NC_000005.9:g.110407417G= , CM000667.1:g.110407417G= | GRCh37 |
| NC_000005.8:g.110435316G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.-172G= MANE Select | ENSP00000339804.3:n.-172G= | |
| ENST00000344895.3:c.-172G= | ENSP00000339804.3:n.-172G= | |
| ENST00000420978.6:c.34+202G= | ENSP00000399099.2:n.34+202G= | |
| NM_033035.4:c.-172G= | NP_149024.1:n.-172G= | |
| NR_045089.1:n.1438+202G= | ||
| NM_033035.5:c.-172G= MANE Select | NP_149024.1:n.-172G= | |
| NR_045089.2:n.1456+202G= |