Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24306035A>T , CM000668.2:g.24306035A>T | GRCh38 |
| NC_000006.11:g.24306263A>T , CM000668.1:g.24306263A>T | GRCh37 |
| NC_000006.10:g.24414242A>T | NCBI36 |
| NG_012829.1:g.57018T>A | |
| NG_012829.2:g.82258T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.349-3991T>A MANE Select | ENSP00000367715.3:n.349-3991T>A | |
| ENST00000378454.7:c.349-3991T>A | ENSP00000367715.3:n.349-3991T>A | |
| NM_001195610.1:c.349-3991T>A | NP_001182539.1:n.349-3991T>A | |
| NM_016356.4:c.349-3991T>A | NP_057440.2:n.349-3991T>A | |
| NM_016356.5:c.349-3991T>A MANE Select | NP_057440.2:n.349-3991T>A | |
| NM_001195610.2:c.349-3991T>A | NP_001182539.1:n.349-3991T>A |