dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21774926A>T , CM000684.2:g.21774926A>T | GRCh38 |
| NC_000022.10:g.22129215A>T , CM000684.1:g.22129215A>T | GRCh37 |
| NC_000022.9:g.20459215A>T | NCBI36 |
| NG_023054.2:g.97755T>A , LRG_786:g.97755T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215832.11:c.857-1944T>A MANE Select | ENSP00000215832.7:n.857-1944T>A | |
| ENST00000215832.10:c.857-1944T>A | ENSP00000215832.6:n.857-1944T>A | |
| ENST00000398822.7:c.857-1944T>A | ENSP00000381803.3:n.857-1944T>A | |
| ENST00000544786.1:c.725-1944T>A | ENSP00000440842.1:n.725-1944T>A | |
| NM_002745.4:c.857-1944T>A , LRG_786t1:c.857-1944T>A | NP_002736.3:n.857-1944T>A | |
| NM_138957.3:c.857-1944T>A , LRG_786t2:c.857-1944T>A | NP_620407.1:n.857-1944T>A | |
| NM_002745.5:c.857-1944T>A MANE Select | NP_002736.3:n.857-1944T>A |