Linked Data
dbSNP Id:
rs2134695053
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.110460936_110460941dup , CM000673.2:g.110460936_110460941dup | GRCh38 |
| NC_000011.9:g.110331660_110331665dup , CM000673.1:g.110331660_110331665dup | GRCh37 |
| NC_000011.8:g.109836870_109836875dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260270.3:c.441-1418_441-1413dup MANE Select | ENSP00000260270.2:n.441-1418_441-1413dup | |
| ENST00000260270.2:c.441-1418_441-1413dup | ENSP00000260270.2:n.441-1418_441-1413dup | |
| NM_004109.4:c.441-1418_441-1413dup | NP_004100.1:n.441-1418_441-1413dup | |
| NM_004109.5:c.441-1418_441-1413dup MANE Select | NP_004100.1:n.441-1418_441-1413dup |