Linked Data
dbSNP Id:
rs1254645690
gnomAD v2:
11-6411598-C-T
gnomAD v3:
11-6390368-C-T
gnomAD v4:
11-6390368-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390368C>T , CM000673.2:g.6390368C>T | GRCh38 |
| NC_000011.9:g.6411598C>T , CM000673.1:g.6411598C>T | GRCh37 |
| NC_000011.8:g.6368174C>T | NCBI36 |
| NG_011780.1:g.4944C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_005253075.3:c.-231C>T | XP_005253132.1:n.-231C>T | |
| XM_011520303.1:c.-231C>T | XP_011518605.1:n.-231C>T | |
| XM_011520304.1:c.-231C>T | XP_011518606.1:n.-231C>T | |
| XR_930886.1:n.68C>T |