Linked Data
dbSNP Id:
rs2102227849
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.159301939T>C , CM000663.2:g.159301939T>C | GRCh38 |
| NC_000001.10:g.159271729T>C , CM000663.1:g.159271729T>C | GRCh37 |
| NC_000001.9:g.157538353T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000368115.5:c.-59-367T>C | ENSP00000357097.1:n.-59-367T>C | |
| NM_002001.3:c.-59-367T>C | NP_001992.1:n.-59-367T>C | |
| NM_002001.4:c.-59-367T>C | NP_001992.1:n.-59-367T>C |