Linked Data
ClinVar Variation Id:
457889
ClinVar RCV Id:
RCV000538145
dbSNP Id:
rs1556000763
gnomAD v4:
22-29673270-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29673270T>C , CM000684.2:g.29673270T>C | GRCh38 |
| NC_000022.10:g.30069259T>C , CM000684.1:g.30069259T>C | GRCh37 |
| NC_000022.9:g.28399259T>C | NCBI36 |
| NG_009057.1:g.74715T>C , LRG_511:g.74715T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361166.10:c.989T>C | ENSP00000354529.6:p.Met330Thr | |
| ENST00000673312.2:c.*618T>C | ENSP00000500186.2:n.*618T>C | |
| ENST00000338641.10:c.1124T>C MANE Select | ENSP00000344666.5:p.Met375Thr | |
| ENST00000361166.9:c.542T>C | ENSP00000354529.5:p.Met181Thr | |
| ENST00000672461.1:c.1124T>C | ENSP00000500919.1:p.Met375Thr | |
| ENST00000672805.1:c.*1006T>C | ENSP00000500295.1:n.*1006T>C | |
| ENST00000672896.1:c.1124T>C | ENSP00000500117.1:p.Met375Thr | |
| ENST00000673312.1:c.1143T>C | ENSP00000500186.1:n.1143T>C | |
| ENST00000334961.11:c.875T>C | ENSP00000335652.7:p.Met292Thr | |
| ENST00000338641.8:c.1124T>C | ENSP00000344666.4:p.Met375Thr | |
| ENST00000353887.8:c.875T>C | ENSP00000340626.4:p.Met292Thr | |
| ENST00000361166.8:c.1124T>C | ENSP00000354529.4:p.Met375Thr | |
| ENST00000361452.8:c.1001T>C | ENSP00000354897.4:p.Met334Thr | |
| ENST00000361676.8:c.998T>C | ENSP00000355183.4:p.Met333Thr | |
| ENST00000397789.3:c.1124T>C | ENSP00000380891.3:p.Met375Thr | |
| ENST00000403435.5:c.1037T>C | ENSP00000384029.1:p.Met346Thr | |
| ENST00000403999.7:c.1124T>C | ENSP00000384797.3:p.Met375Thr | |
| ENST00000413209.6:c.448-21482T>C | ENSP00000409921.2:n.448-21482T>C | |
| ENST00000432151.5:c.523-1566T>C | ENSP00000395885.1:n.523-1566T>C | |
| NM_000268.3:c.1124T>C , LRG_511t1:c.1124T>C | NP_000259.1:p.Met375Thr | |
| NM_016418.5:c.1124T>C , LRG_511t2:c.1124T>C | NP_057502.2:p.Met375Thr | |
| NM_181825.2:c.1124T>C | NP_861546.1:p.Met375Thr | |
| NM_181828.2:c.998T>C | NP_861966.1:p.Met333Thr | |
| NM_181829.2:c.1001T>C | NP_861967.1:p.Met334Thr | |
| NM_181830.2:c.875T>C | NP_861968.1:p.Met292Thr | |
| NM_181831.2:c.875T>C | NP_861969.1:p.Met292Thr | |
| NM_181832.2:c.1124T>C | NP_861970.1:p.Met375Thr | |
| NM_181833.2:c.448-21482T>C | NP_861971.1:n.448-21482T>C | |
| NR_156186.1:n.1683T>C | ||
| XM_017028809.2:c.1010T>C | XP_016884298.1:p.Met337Thr | |
| XM_017028810.1:c.1010T>C | XP_016884299.1:p.Met337Thr | |
| NM_000268.4:c.1124T>C MANE Select | NP_000259.1:p.Met375Thr | |
| NM_181825.3:c.1124T>C | NP_861546.1:p.Met375Thr | |
| NM_181828.3:c.998T>C | NP_861966.1:p.Met333Thr | |
| NM_181829.3:c.1001T>C | NP_861967.1:p.Met334Thr | |
| NM_181830.3:c.875T>C | NP_861968.1:p.Met292Thr | |
| NM_181831.3:c.875T>C | NP_861969.1:p.Met292Thr | |
| NM_181832.3:c.1124T>C | NP_861970.1:p.Met375Thr | |
| NR_156186.2:n.1606T>C | ||
| NM_181833.3:c.448-21482T>C | NP_861971.1:n.448-21482T>C |