Linked Data
dbSNP Id:
rs35783848
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10644083dup , CM000682.2:g.10644083dup | GRCh38 |
| NC_000020.10:g.10624731dup , CM000682.1:g.10624731dup | GRCh37 |
| NC_000020.9:g.10572731dup | NCBI36 |
| NG_007496.1:g.34966dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2373-218dup MANE Select | ENSP00000254958.4:n.2373-218dup | |
| ENST00000617965.2:n.2962-218dup | ||
| ENST00000254958.9:c.2373-218dup | ENSP00000254958.4:n.2373-218dup | |
| ENST00000423891.6:n.2239-218dup | ||
| NM_000214.2:c.2373-218dup | NP_000205.1:n.2373-218dup | |
| NM_000214.3:c.2373-218dup MANE Select | NP_000205.1:n.2373-218dup |