Linked Data
dbSNP Id:
rs12429889
gnomAD v2:
13-74742322-T-C
gnomAD v3:
13-74168185-T-C
gnomAD v4:
13-74168185-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.74168185T>C , CM000675.2:g.74168185T>C | GRCh38 |
| NC_000013.10:g.74742322T>C , CM000675.1:g.74742322T>C | GRCh37 |
| NC_000013.9:g.73640323T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011534909.2:c.-68A>G | XP_011533211.1:n.-68A>G | |
| NM_001400139.1:c.-32+137811A>G | NP_001387068.1:n.-32+137811A>G | |
| NM_001400153.1:c.-32+137811A>G | NP_001387082.1:n.-32+137811A>G |