Linked Data
dbSNP Id:
rs1939970080
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52814325A>G , CM000674.2:g.52814325A>G | GRCh38 |
| NC_000012.11:g.53208109A>G , CM000674.1:g.53208109A>G | GRCh37 |
| NC_000012.10:g.51494376A>G | NCBI36 |
| NG_007380.1:g.5227T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000551956.1:c.-267T>C | ENSP00000448220.1:n.-267T>C |