Linked Data
dbSNP Id:
rs2092604320
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149928136A>G , CM000663.2:g.149928136A>G | GRCh38 |
| NC_000001.10:g.149900028A>G , CM000663.1:g.149900028A>G | GRCh37 |
| NC_000001.9:g.148166652A>G | NCBI36 |
| NG_032777.1:g.5117T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-377T>C | ENSP00000271628.8:n.-377T>C | |
| NM_005850.4:c.-377T>C | NP_005841.1:n.-377T>C |