Linked Data
dbSNP Id:
rs10177924
gnomAD v2:
2-156933553-A-G
gnomAD v3:
2-156077041-A-G
gnomAD v4:
2-156077041-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.156077041A>G , CM000664.2:g.156077041A>G | GRCh38 |
| NC_000002.11:g.156933553A>G , CM000664.1:g.156933553A>G | GRCh37 |
| NC_000002.10:g.156641799A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_110249.2:n.155-52465T>C | ||
| NR_110250.2:n.155-52434T>C |