Linked Data
dbSNP Id:
rs1560188348
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24794877T>C , CM000666.2:g.24794877T>C | GRCh38 |
| NC_000004.11:g.24796499T>C , CM000666.1:g.24796499T>C | GRCh37 |
| NC_000004.10:g.24405597T>C | NCBI36 |
| NG_012213.1:g.4415T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000598411.1:c.-16-4629T>C | ENSP00000472134.1:n.-16-4629T>C |