Linked Data
dbSNP Id:
rs1036765817
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762645A>C , CM000672.2:g.94762645A>C | GRCh38 |
| NC_000010.10:g.96522402A>C , CM000672.1:g.96522402A>C | GRCh37 |
| NC_000010.9:g.96512392A>C | NCBI36 |
| NG_008384.2:g.4940A>C | |
| NG_008384.3:g.4965A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371321.7:c.-61A>C | ENSP00000360372.3:n.-61A>C | |
| ENST00000464755.1:c.932-12413A>C | ENSP00000483243.1:n.932-12413A>C |