Linked Data
ClinVar Variation Id:
99876
dbSNP Id:
rs62636267
gnomAD v2:
1-197396677-T-C
gnomAD v4:
1-197427547-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197427547T>C , CM000663.2:g.197427547T>C | GRCh38 |
| NC_000001.10:g.197396677T>C , CM000663.1:g.197396677T>C | GRCh37 |
| NC_000001.9:g.195663300T>C | NCBI36 |
| NG_008483.1:g.164270T>C | |
| NG_008483.2:g.231086T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.2222T>C MANE Select | ENSP00000356370.3:p.Met741Thr | |
| ENST00000638467.1:c.2222T>C | ENSP00000491102.1:p.Met741Thr | |
| ENST00000681519.1:c.1103T>C | ENSP00000505267.1:p.Met368Thr | |
| ENST00000367397.1:c.365T>C | ENSP00000356367.1:p.Met122Thr | |
| ENST00000367399.6:c.1886T>C | ENSP00000356369.2:p.Met629Thr | |
| ENST00000367400.7:c.2222T>C | ENSP00000356370.3:p.Met741Thr | |
| ENST00000480086.2:n.123T>C | ||
| ENST00000484075.5:c.2222T>C | ENSP00000433932.1:p.Met741Thr | |
| ENST00000535699.5:c.2015T>C | ENSP00000438786.1:p.Met672Thr | |
| ENST00000538660.5:c.2128+5591T>C | ENSP00000438091.1:n.2128+5591T>C | |
| NM_001193640.1:c.1886T>C | NP_001180569.1:p.Met629Thr | |
| NM_001257965.1:c.2015T>C | NP_001244894.1:p.Met672Thr | |
| NM_001257966.1:c.2128+5591T>C | NP_001244895.1:n.2128+5591T>C | |
| NM_201253.2:c.2222T>C | NP_957705.1:p.Met741Thr | |
| NR_047563.1:n.2223T>C | ||
| NR_047564.1:n.2431T>C | ||
| XM_011509365.1:c.2222T>C | XP_011507667.1:p.Met741Thr | |
| XM_011509366.1:c.2222T>C | XP_011507668.1:p.Met741Thr | |
| XM_011509367.1:c.2222T>C | XP_011507669.1:p.Met741Thr | |
| XM_011509368.1:c.1640T>C | XP_011507670.1:p.Met547Thr | |
| XM_011509369.1:c.665T>C | XP_011507671.1:p.Met222Thr | |
| XM_011509365.2:c.2222T>C | XP_011507667.1:p.Met741Thr | |
| XM_011509369.2:c.665T>C | XP_011507671.1:p.Met222Thr | |
| XM_017000851.1:c.1379T>C | XP_016856340.1:p.Met460Thr | |
| XM_017000852.1:c.2222T>C | XP_016856341.1:p.Met741Thr | |
| NM_201253.3:c.2222T>C MANE Select | NP_957705.1:p.Met741Thr | |
| NM_001193640.2:c.1886T>C | NP_001180569.1:p.Met629Thr | |
| NM_001257965.2:c.2015T>C | NP_001244894.1:p.Met672Thr | |
| NR_047563.2:n.2175T>C | ||
| NR_047564.2:n.2383T>C | ||
| NM_001257966.2:c.2128+5591T>C | NP_001244895.1:n.2128+5591T>C |