Linked Data
dbSNP Id:
rs2144968246
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.77268552_77268553insATC , CM000680.2:g.77268552_77268553insATC | GRCh38 |
| NC_000018.9:g.74980508_74980509insATC , CM000680.1:g.74980508_74980509insATC | GRCh37 |
| NC_000018.8:g.73109496_73109497insATC | NCBI36 |
| NG_009223.1:g.23501_23502insATC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299727.5:c.733-33_733-32insATC MANE Select | ENSP00000299727.3:n.733-33_733-32insATC | |
| ENST00000299727.4:c.733-33_733-32insATC | ENSP00000299727.3:n.733-33_733-32insATC | |
| NM_001480.3:c.733-33_733-32insATC | NP_001471.2:n.733-33_733-32insATC | |
| NM_001480.4:c.733-33_733-32insATC MANE Select | NP_001471.2:n.733-33_733-32insATC |