Linked Data
dbSNP Id:
rs2111179622
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.139874121T>G , CM000666.2:g.139874121T>G | GRCh38 |
| NC_000004.11:g.140795275T>G , CM000666.1:g.140795275T>G | GRCh37 |
| NC_000004.10:g.141014725T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502696.1:c.111-143454A>C | ||
| ENST00000509479.6:c.2079+15236A>C MANE Select | ENSP00000421180.1:n.2079+15236A>C | |
| NM_018717.4:c.2067+15236A>C | NP_061187.2:n.2067+15236A>C | |
| NM_018717.5:c.2079+15236A>C MANE Select | NP_061187.3:n.2079+15236A>C |