Linked Data
gnomAD v4:
22-42130978-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42130978A>G , CM000684.2:g.42130978A>G | GRCh38 |
| NC_000022.10:g.42526980A>G , CM000684.1:g.42526980A>G | GRCh37 |
| NC_000022.9:g.40856924A>G | NCBI36 |
| NG_008376.3:g.4014T>C | |
| NG_008376.4:g.4833T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011529966.1:c.-187T>C | XP_011528268.1:n.-187T>C | |
| XM_011529967.1:c.-187T>C | XP_011528269.1:n.-187T>C | |
| XM_011529968.1:c.-187T>C | XP_011528270.1:n.-187T>C | |
| XM_011529969.1:c.37+319T>C | XP_011528271.1:n.37+319T>C | |
| XM_011529970.1:c.-187T>C | XP_011528272.1:n.-187T>C | |
| XM_011529971.1:c.37+319T>C | XP_011528273.1:n.37+319T>C | |
| XM_011529972.1:c.-187T>C | XP_011528274.1:n.-187T>C | |
| XR_430455.2:n.328+290A>G | ||
| XR_002958749.1:n.275+290A>G |