Linked Data
dbSNP Id:
rs1326012812
gnomAD v2:
5-150240346-C-G
gnomAD v3:
5-150860784-C-G
gnomAD v4:
5-150860784-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150860784C>G , CM000667.2:g.150860784C>G | GRCh38 |
| NC_000005.9:g.150240346C>G , CM000667.1:g.150240346C>G | GRCh37 |
| NC_000005.8:g.150220539C>G | NCBI36 |
| NG_027809.2:g.19262C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000520549.1:c.158+12130C>G | ||
| XM_011537641.1:c.531+12130C>G | XP_011535943.1:n.531+12130C>G | |
| NM_001346557.1:c.531+12130C>G | NP_001333486.1:n.531+12130C>G | |
| NM_001346557.2:c.531+12130C>G | NP_001333486.1:n.531+12130C>G | |
| NR_170598.1:n.1646+12130C>G |