Linked Data
dbSNP Id:
rs35481113
gnomAD v2:
22-42527018-T-C
gnomAD v3:
22-42131016-T-C
gnomAD v4:
22-42131016-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42131016T>C , CM000684.2:g.42131016T>C | GRCh38 |
| NC_000022.10:g.42527018T>C , CM000684.1:g.42527018T>C | GRCh37 |
| NC_000022.9:g.40856962T>C | NCBI36 |
| NG_008376.3:g.3976A>G | |
| NG_008376.4:g.4795A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011529966.1:c.-225A>G | XP_011528268.1:n.-225A>G | |
| XM_011529967.1:c.-225A>G | XP_011528269.1:n.-225A>G | |
| XM_011529968.1:c.-225A>G | XP_011528270.1:n.-225A>G | |
| XM_011529969.1:c.37+281A>G | XP_011528271.1:n.37+281A>G | |
| XM_011529970.1:c.-225A>G | XP_011528272.1:n.-225A>G | |
| XM_011529971.1:c.37+281A>G | XP_011528273.1:n.37+281A>G | |
| XM_011529972.1:c.-225A>G | XP_011528274.1:n.-225A>G | |
| XR_430455.2:n.328+328T>C | ||
| XR_002958749.1:n.275+328T>C |