Linked Data
dbSNP Id:
rs1827946513
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101585988A>G , CM000671.2:g.101585988A>G | GRCh38 |
| NC_000009.11:g.104348270A>G , CM000671.1:g.104348270A>G | GRCh37 |
| NC_000009.10:g.103388091A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361820.6:c.2767-6628T>C MANE Select | ENSP00000355155.3:n.2767-6628T>C | |
| ENST00000361820.3:c.2767-6628T>C | ENSP00000355155.3:n.2767-6628T>C | |
| NM_133445.2:c.2767-6628T>C | NP_597702.2:n.2767-6628T>C | |
| NM_133445.3:c.2767-6628T>C MANE Select | NP_597702.2:n.2767-6628T>C |