Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8016204G= , CM000679.2:g.8016204G= | GRCh38 |
| NC_000017.10:g.7919522G= , CM000679.1:g.7919522G= | GRCh37 |
| NC_000017.9:g.7860247G= | NCBI36 |
| NG_009092.1:g.18535G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000180.4:c.3139-1G= MANE Select | NP_000171.1:n.3139-1G= |
| ENST00000254854.5:c.3139-1G= MANE Select | ENSP00000254854.4:n.3139-1G= |
| NM_000180.3:c.3139-1G= | NP_000171.1:n.3139-1G= |
| ENST00000254854.4:c.3139-1G= | ENSP00000254854.4:n.3139-1G= |
| ENST00000574510.1:n.76G= | |
| XM_011523816.1:c.3139-1G= | XP_011522118.1:n.3139-1G= |