dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.72004363A>T , CM000674.2:g.72004363A>T | GRCh38 |
| NC_000012.11:g.72398143A>T , CM000674.1:g.72398143A>T | GRCh37 |
| NC_000012.10:g.70684410A>T | NCBI36 |
| NG_008279.1:g.70518A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333850.4:c.1068+9798A>T MANE Select | ENSP00000329093.3:n.1068+9798A>T | |
| ENST00000333850.3:c.1068+9798A>T | ENSP00000329093.3:n.1068+9798A>T | |
| NM_173353.3:c.1068+9798A>T | NP_775489.2:n.1068+9798A>T | |
| XM_011537899.1:c.474+9798A>T | XP_011536201.1:n.474+9798A>T | |
| NM_173353.4:c.1068+9798A>T MANE Select | NP_775489.2:n.1068+9798A>T |