Linked Data
dbSNP Id:
rs1182269623
gnomAD v2:
X-140983451-G-C
gnomAD v3:
X-141895665-G-C
gnomAD v4:
X-141895665-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.141895665G>C , CM000685.2:g.141895665G>C | GRCh38 |
| NC_000023.10:g.140983451G>C , CM000685.1:g.140983451G>C | GRCh37 |
| NC_000023.9:g.140811117G>C | NCBI36 |
| NG_013272.1:g.62350G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298296.1:c.1123+106G>C MANE Select | ENSP00000298296.1:n.1123+106G>C | |
| ENST00000443323.2:c.-118-766G>C | ENSP00000438254.1:n.-118-766G>C | |
| ENST00000483584.5:n.288+258G>C | ||
| ENST00000544766.5:c.-240+258G>C | ENSP00000440444.1:n.-240+258G>C | |
| NM_138702.1:c.1123+106G>C MANE Select | NP_619647.1:n.1123+106G>C | |
| NM_177456.2:c.-240+258G>C | NP_803251.1:n.-240+258G>C | |
| XM_011531267.1:c.-163+258G>C | XP_011529569.1:n.-163+258G>C | |
| XM_011531267.3:c.-163+258G>C | XP_011529569.1:n.-163+258G>C | |
| XM_017029265.2:c.-240+258G>C | XP_016884754.1:n.-240+258G>C |