Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.27489253A>C , CM000671.2:g.27489253A>C | GRCh38 |
| NC_000009.11:g.27489251A>C , CM000671.1:g.27489251A>C | GRCh37 |
| NC_000009.10:g.27479251A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024761.5:c.-198-33505T>G MANE Select | NP_079037.3:n.-198-33505T>G |
| ENST00000262244.6:c.-198-33505T>G MANE Select | ENSP00000262244.5:n.-198-33505T>G |
| NM_024761.4:c.-198-33505T>G | NP_079037.3:n.-198-33505T>G |
| ENST00000262244.5:c.-198-33505T>G | ENSP00000262244.5:n.-198-33505T>G |