Linked Data
dbSNP Id:
rs904322263
gnomAD v4:
22-32475113-C-G
MyVariant Identifiers:
chr22:g.32871100C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32475113C>G , CM000684.2:g.32475113C>G | GRCh38 |
| NC_000022.10:g.32871100C>G , CM000684.1:g.32871100C>G | GRCh37 |
| NC_000022.9:g.31201100C>G | NCBI36 |
| NG_016001.1:g.5394C>G | |
| NG_016001.2:g.5394C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.111C>G MANE Select | ENSP00000266087.7:p.Thr37= | |
| ENST00000266087.11:c.111C>G | ENSP00000266087.7:p.Thr37= | |
| ENST00000420700.5:c.111C>G | ENSP00000406155.1:p.Thr37= | |
| ENST00000425028.5:c.111C>G | ENSP00000395823.1:p.Thr37= | |
| ENST00000492535.1:n.99C>G | ||
| NM_012179.3:c.111C>G | NP_036311.3:p.Thr37= | |
| XM_011530106.1:c.-63C>G | XP_011528408.1:n.-63C>G | |
| XM_024452207.1:c.-80C>G | XP_024307975.1:n.-80C>G | |
| NM_012179.4:c.111C>G MANE Select | NP_036311.3:p.Thr37= |