Linked Data
dbSNP Id:
rs113182869
gnomAD v2:
20-44576493-T-C
gnomAD v3:
20-45947854-T-C
gnomAD v4:
20-45947854-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.45947854T>C , CM000682.2:g.45947854T>C | GRCh38 |
| NC_000020.10:g.44576493T>C , CM000682.1:g.44576493T>C | GRCh37 |
| NC_000020.9:g.44009900T>C | NCBI36 |
| NG_029772.1:g.29341A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372409.8:c.*99T>C MANE Select | ENSP00000361486.3:n.*99T>C | |
| ENST00000372409.7:c.*99T>C | ENSP00000361486.3:n.*99T>C | |
| ENST00000479348.2:c.1155T>C | ||
| NM_022104.3:c.*99T>C | NP_071387.1:n.*99T>C | |
| XM_011528980.1:c.*99T>C | XP_011527282.1:n.*99T>C | |
| XM_011528981.1:c.*99T>C | XP_011527283.1:n.*99T>C | |
| XM_011528982.1:c.*99T>C | XP_011527284.1:n.*99T>C | |
| XM_011528980.3:c.*99T>C | XP_011527282.1:n.*99T>C | |
| XM_011528981.3:c.*99T>C | XP_011527283.1:n.*99T>C | |
| XM_017028013.2:c.*99T>C | XP_016883502.1:n.*99T>C | |
| XM_017028014.2:c.*99T>C | XP_016883503.1:n.*99T>C | |
| NM_022104.4:c.*99T>C MANE Select | NP_071387.1:n.*99T>C |