Linked Data
dbSNP Id:
rs965724048
gnomAD v4:
10-17129840-C-T
MyVariant Identifiers:
chr10:g.17129840C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17129840C>T , CM000672.2:g.17129840C>T | GRCh38 |
| NC_000010.10:g.17171839C>T , CM000672.1:g.17171839C>T | GRCh37 |
| NC_000010.9:g.17211845C>T | NCBI36 |
| NG_008967.1:g.4978G>A , LRG_540:g.4978G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519708.1:c.-75G>A | XP_011518010.1:n.-75G>A | |
| XM_011519708.2:c.-75G>A | XP_011518010.1:n.-75G>A |