Linked Data
dbSNP Id:
rs1589952664
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133527168A>C , CM000672.2:g.133527168A>C | GRCh38 |
| NC_000010.10:g.135340672A>C , CM000672.1:g.135340672A>C | GRCh37 |
| NC_000010.9:g.135190662A>C | NCBI36 |
| NG_008383.1:g.4806A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463117.6:c.-39-189A>C | ENSP00000440689.1:n.-39-189A>C | |
| ENST00000541261.1:c.-39-189A>C | ENSP00000437799.1:n.-39-189A>C |