Linked Data
dbSNP Id:
rs768078854
ExAC:
19:17940948 C / G
gnomAD v2:
19-17940948-C-G
gnomAD v4:
19-17830139-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17830139C>G , CM000681.2:g.17830139C>G | GRCh38 |
| NC_000019.9:g.17940948C>G , CM000681.1:g.17940948C>G | GRCh37 |
| NC_000019.8:g.17801948C>G | NCBI36 |
| NG_007273.1:g.22853G>C , LRG_77:g.22853G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526008.6:c.*1733G>C | ENSP00000513006.1:n.*1733G>C | |
| ENST00000696967.1:n.2353G>C | ||
| ENST00000696968.1:n.409G>C | ||
| ENST00000696969.1:n.2133G>C | ||
| ENST00000458235.7:c.3176G>C MANE Select | ENSP00000391676.1:p.Arg1059Thr | |
| ENST00000458235.5:c.3176G>C | ENSP00000391676.1:p.Arg1059Thr | |
| ENST00000527031.5:n.2279-4829G>C | ||
| ENST00000527670.5:c.3176G>C | ENSP00000432511.1:p.Arg1059Thr | |
| ENST00000534444.1:c.3176G>C | ENSP00000436421.1:p.Arg1059Thr | |
| NM_000215.3:c.3176G>C , LRG_77t1:c.3176G>C | NP_000206.2:p.Arg1059Thr | |
| XM_005259896.2:c.3305G>C | XP_005259953.1:p.Arg1102Thr | |
| XM_006722745.2:c.3176G>C | XP_006722808.1:p.Arg1059Thr | |
| XM_005259896.3:c.3305G>C | XP_005259953.1:p.Arg1102Thr | |
| NM_000215.4:c.3176G>C MANE Select | NP_000206.2:p.Arg1059Thr |