Linked Data
dbSNP Id:
rs3865444
gnomAD v2:
19-51727962-C-A
gnomAD v3:
19-51224706-C-A
gnomAD v4:
19-51224706-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.51224706C>A , CM000681.2:g.51224706C>A | GRCh38 |
| NC_000019.9:g.51727962C>A , CM000681.1:g.51727962C>A | GRCh37 |
| NC_000019.8:g.56419774C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011527531.1:c.-1C>A | XP_011525833.1:n.-1C>A | |
| XM_011527532.1:c.-38C>A | XP_011525834.1:n.-38C>A | |
| XR_935875.1:n.72C>A | ||
| XM_011527531.2:c.-1C>A | XP_011525833.1:n.-1C>A | |
| XM_011527532.2:c.-38C>A | XP_011525834.1:n.-38C>A | |
| XM_017027508.1:c.-1C>A | XP_016882997.1:n.-1C>A | |
| XM_017027509.1:c.-1C>A | XP_016882998.1:n.-1C>A | |
| XM_017027510.1:c.-1C>A | XP_016882999.1:n.-1C>A |