Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8011982T>C , CM000679.2:g.8011982T>C | GRCh38 |
| NC_000017.10:g.7915300T>C , CM000679.1:g.7915300T>C | GRCh37 |
| NC_000017.9:g.7856025T>C | NCBI36 |
| NG_009092.1:g.14313T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.1750-162T>C MANE Select | ENSP00000254854.4:n.1750-162T>C | |
| ENST00000254854.4:c.1750-162T>C | ENSP00000254854.4:n.1750-162T>C | |
| NM_000180.3:c.1750-162T>C | NP_000171.1:n.1750-162T>C | |
| XM_011523816.1:c.1750-162T>C | XP_011522118.1:n.1750-162T>C | |
| NM_000180.4:c.1750-162T>C MANE Select | NP_000171.1:n.1750-162T>C |