Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63065902A>T , CM000670.2:g.63065902A>T | GRCh38 |
| NC_000008.10:g.63978461A>T , CM000670.1:g.63978461A>T | GRCh37 |
| NC_000008.9:g.64141015A>T | NCBI36 |
| NG_016123.1:g.25152T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000370.3:c.552+2T>A MANE Select | NP_000361.1:n.552+2T>A |
| ENST00000260116.5:c.552+2T>A MANE Select | ENSP00000260116.4:n.552+2T>A |
| ENST00000260116.4:c.552+2T>A | ENSP00000260116.4:n.552+2T>A |
| ENST00000521138.1:n.233-17299T>A | |
| XM_006716468.2:c.205-1586T>A | XP_006716531.1:n.205-1586T>A |
| XM_006716468.4:c.205-1586T>A | XP_006716531.1:n.205-1586T>A |