Linked Data
dbSNP Id:
rs977201535
gnomAD v4:
10-17129862-T-C
MyVariant Identifiers:
chr10:g.17129862T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17129862T>C , CM000672.2:g.17129862T>C | GRCh38 |
| NC_000010.10:g.17171861T>C , CM000672.1:g.17171861T>C | GRCh37 |
| NC_000010.9:g.17211867T>C | NCBI36 |
| NG_008967.1:g.4956A>G , LRG_540:g.4956A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519708.1:c.-97A>G | XP_011518010.1:n.-97A>G | |
| XM_011519708.2:c.-97A>G | XP_011518010.1:n.-97A>G |