Linked Data
dbSNP Id:
rs2037490881
gnomAD v4:
15-90966388-C-T
MyVariant Identifiers:
chr15:g.91509618C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90966388C>T , CM000677.2:g.90966388C>T | GRCh38 |
| NC_000015.9:g.91509618C>T , CM000677.1:g.91509618C>T | GRCh37 |
| NC_000015.8:g.89310622C>T | NCBI36 |
| NG_050647.1:g.33264G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394249.8:c.*743G>A (PRC1) MANE Select | ENSP00000377793.3:n.*743G>A | |
| ENST00000643536.1:c.*4368G>A | ENSP00000494429.1:n.*4368G>A | |
| ENST00000361188.9:c.*743G>A (PRC1) | ENSP00000354679.5:n.*743G>A | |
| ENST00000394249.7:c.*743G>A (PRC1) | ENSP00000377793.3:n.*743G>A | |
| ENST00000556972.6:c.390G>A (PRC1) | ENSP00000456737.1:n.390G>A | |
| NM_001267580.1:c.*786G>A (PRC1) | NP_001254509.1:n.*786G>A | |
| NM_003981.3:c.*743G>A (PRC1) | NP_003972.1:n.*743G>A | |
| NM_199413.2:c.*743G>A (PRC1) | NP_955445.1:n.*743G>A | |
| NR_051984.1:n.20C>T (PRC1-AS1) | ||
| XM_005254987.1:c.*786G>A (PRC1) | XP_005255044.1:n.*786G>A | |
| XM_006720759.1:c.*837G>A (PRC1) | XP_006720822.1:n.*837G>A | |
| XM_006720760.1:c.*249G>A (PRC1) | XP_006720823.1:n.*249G>A | |
| XM_011522187.1:c.*191G>A (PRC1) | XP_011520489.1:n.*191G>A | |
| XM_011522188.1:c.*191G>A (PRC1) | XP_011520490.1:n.*191G>A | |
| XM_011522189.1:c.*191G>A (PRC1) | XP_011520491.1:n.*191G>A | |
| XM_011522190.1:c.*191G>A (PRC1) | XP_011520492.1:n.*191G>A | |
| XM_011522192.1:c.*191G>A (PRC1) | XP_011520494.1:n.*191G>A | |
| XM_005254987.3:c.*786G>A (PRC1) | XP_005255044.1:n.*786G>A | |
| XM_006720759.2:c.*837G>A (PRC1) | XP_006720822.1:n.*837G>A | |
| XM_006720760.2:c.*249G>A (PRC1) | XP_006720823.1:n.*249G>A | |
| XM_011522187.2:c.*191G>A (PRC1) | XP_011520489.1:n.*191G>A | |
| XM_011522188.3:c.*191G>A (PRC1) | XP_011520490.1:n.*191G>A | |
| XM_011522189.2:c.*191G>A (PRC1) | XP_011520491.1:n.*191G>A | |
| XM_011522191.3:c.*288G>A (PRC1) | XP_011520493.1:n.*288G>A | |
| XM_011522192.2:c.*191G>A (PRC1) | XP_011520494.1:n.*191G>A | |
| XM_017022712.2:c.*743G>A (PRC1) | XP_016878201.1:n.*743G>A | |
| XM_017022713.2:c.*743G>A (PRC1) | XP_016878202.1:n.*743G>A | |
| XM_017022715.2:c.*743G>A (PRC1) | XP_016878204.1:n.*743G>A | |
| XM_017022716.2:c.*743G>A (PRC1) | XP_016878205.1:n.*743G>A | |
| XM_017022717.1:c.*786G>A (PRC1) | XP_016878206.1:n.*786G>A | |
| NM_003981.4:c.*743G>A (PRC1) MANE Select | NP_003972.2:n.*743G>A | |
| NM_001267580.2:c.*786G>A (PRC1) | NP_001254509.2:n.*786G>A | |
| NM_199413.3:c.*743G>A (PRC1) | NP_955445.2:n.*743G>A |