Linked Data
gnomAD v4:
22-42130969-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42130969G>T , CM000684.2:g.42130969G>T | GRCh38 |
| NC_000022.10:g.42526971G>T , CM000684.1:g.42526971G>T | GRCh37 |
| NC_000022.9:g.40856915G>T | NCBI36 |
| NG_008376.3:g.4023C>A | |
| NG_008376.4:g.4842C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011529966.1:c.-178C>A | XP_011528268.1:n.-178C>A | |
| XM_011529967.1:c.-178C>A | XP_011528269.1:n.-178C>A | |
| XM_011529968.1:c.-178C>A | XP_011528270.1:n.-178C>A | |
| XM_011529969.1:c.37+328C>A | XP_011528271.1:n.37+328C>A | |
| XM_011529970.1:c.-178C>A | XP_011528272.1:n.-178C>A | |
| XM_011529971.1:c.37+328C>A | XP_011528273.1:n.37+328C>A | |
| XM_011529972.1:c.-178C>A | XP_011528274.1:n.-178C>A | |
| XR_430455.2:n.328+281G>T | ||
| XR_002958749.1:n.275+281G>T |