Linked Data
dbSNP Id:
rs2116602002
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155461237T>C , CM000669.2:g.155461237T>C | GRCh38 |
| NC_000007.13:g.155253932T>C , CM000669.1:g.155253932T>C | GRCh37 |
| NC_000007.12:g.154946693T>C | NCBI36 |
| NG_007124.1:g.9518T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297375.4:c.686-1134T>C MANE Select | ENSP00000297375.4:n.686-1134T>C | |
| NM_001427.3:c.686-1134T>C | NP_001418.2:n.686-1134T>C | |
| NM_001427.4:c.686-1134T>C MANE Select | NP_001418.2:n.686-1134T>C |