Linked Data
dbSNP Id:
rs1845905761
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.299485_299486dup , CM000673.2:g.299485_299486dup | GRCh38 |
| NC_000011.9:g.299485_299486dup , CM000673.1:g.299485_299486dup | GRCh37 |
| NC_000011.8:g.289485_289486dup | NCBI36 |
| NG_032892.1:g.5043_5044dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382614.2:c.7_8dup MANE Select | ENSP00000372059.2:p.Ala4ArgfsTer? | |
| NM_001025295.2:c.7_8dup | NP_001020466.1:p.Ala4ArgfsTer? | |
| NM_001025295.3:c.7_8dup MANE Select | NP_001020466.1:p.Ala4ArgfsTer? |