Linked Data
gnomAD v4:
22-42130900-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42130900C>T , CM000684.2:g.42130900C>T | GRCh38 |
| NC_000022.10:g.42526902C>T , CM000684.1:g.42526902C>T | GRCh37 |
| NC_000022.9:g.40856846C>T | NCBI36 |
| NG_008376.3:g.4092G>A | |
| NG_008376.4:g.4911G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360608.9:c.-109G>A | ENSP00000353820.5:n.-109G>A | |
| XM_011529966.1:c.-109G>A | XP_011528268.1:n.-109G>A | |
| XM_011529967.1:c.-109G>A | XP_011528269.1:n.-109G>A | |
| XM_011529968.1:c.-109G>A | XP_011528270.1:n.-109G>A | |
| XM_011529969.1:c.37+397G>A | XP_011528271.1:n.37+397G>A | |
| XM_011529970.1:c.-109G>A | XP_011528272.1:n.-109G>A | |
| XM_011529971.1:c.37+397G>A | XP_011528273.1:n.37+397G>A | |
| XM_011529972.1:c.-109G>A | XP_011528274.1:n.-109G>A | |
| XR_430455.2:n.328+212C>T | ||
| XR_002958749.1:n.275+212C>T |