Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140114165C= , CM000667.2:g.140114165C= | GRCh38 |
| NC_000005.9:g.139493750C= , CM000667.1:g.139493750C= | GRCh37 |
| NC_000005.8:g.139473934C= | NCBI36 |
| NG_041813.1:g.5043C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331327.5:c.-17C= MANE Select | ENSP00000332706.3:n.-17C= | |
| ENST00000505703.2:c.-17C= | ENSP00000498560.1:n.-17C= | |
| ENST00000651386.1:c.-17C= | ENSP00000499133.1:n.-17C= | |
| ENST00000331327.4:c.-17C= | ENSP00000332706.3:n.-17C= | |
| ENST00000502351.1:n.407C= | ||
| ENST00000505703.1:n.449C= | ||
| NM_005859.4:c.-17C= | NP_005850.1:n.-17C= | |
| NM_005859.5:c.-17C= MANE Select | NP_005850.1:n.-17C= |