Linked Data
ClinVar Variation Id:
5730
ClinVar RCV Id:
RCV000006084
RCV000086336
RCV001045972
RCV001250615
RCV001075294
RCV003450614
RCV004528086
dbSNP Id:
rs62635656
gnomAD v2:
1-197404115-T-C
gnomAD v3:
1-197434985-T-C
gnomAD v4:
1-197434985-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197434985T>C , CM000663.2:g.197434985T>C | GRCh38 |
| NC_000001.10:g.197404115T>C , CM000663.1:g.197404115T>C | GRCh37 |
| NC_000001.9:g.195670738T>C | NCBI36 |
| NG_008483.1:g.171708T>C | |
| NG_008483.2:g.238524T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.3122T>C MANE Select | ENSP00000356370.3:p.Met1041Thr | |
| ENST00000638467.1:c.3122T>C | ENSP00000491102.1:p.Met1041Thr | |
| ENST00000681519.1:c.2003T>C | ENSP00000505267.1:p.Met668Thr | |
| ENST00000367397.1:c.1265T>C | ENSP00000356367.1:p.Met422Thr | |
| ENST00000367399.6:c.2786T>C | ENSP00000356369.2:p.Met929Thr | |
| ENST00000367400.7:c.3122T>C | ENSP00000356370.3:p.Met1041Thr | |
| ENST00000484075.5:c.3122T>C | ENSP00000433932.1:p.Met1041Thr | |
| ENST00000535699.5:c.3050T>C | ENSP00000438786.1:p.Met1017Thr | |
| ENST00000538660.5:c.2129-615T>C | ENSP00000438091.1:n.2129-615T>C | |
| NM_001193640.1:c.2786T>C | NP_001180569.1:p.Met929Thr | |
| NM_001257965.1:c.3050T>C | NP_001244894.1:p.Met1017Thr | |
| NM_001257966.1:c.2129-615T>C | NP_001244895.1:n.2129-615T>C | |
| NM_201253.2:c.3122T>C | NP_957705.1:p.Met1041Thr | |
| NR_047563.1:n.3123T>C | ||
| NR_047564.1:n.3331T>C | ||
| XM_011509365.1:c.3122T>C | XP_011507667.1:p.Met1041Thr | |
| XM_011509366.1:c.3122T>C | XP_011507668.1:p.Met1041Thr | |
| XM_011509367.1:c.3122T>C | XP_011507669.1:p.Met1041Thr | |
| XM_011509368.1:c.2540T>C | XP_011507670.1:p.Met847Thr | |
| XM_011509369.1:c.1565T>C | XP_011507671.1:p.Met522Thr | |
| XM_011509365.2:c.3122T>C | XP_011507667.1:p.Met1041Thr | |
| XM_011509369.2:c.1565T>C | XP_011507671.1:p.Met522Thr | |
| XM_017000851.1:c.2279T>C | XP_016856340.1:p.Met760Thr | |
| XM_017000852.1:c.3257T>C | XP_016856341.1:p.Met1086Thr | |
| NM_201253.3:c.3122T>C MANE Select | NP_957705.1:p.Met1041Thr | |
| NM_001193640.2:c.2786T>C | NP_001180569.1:p.Met929Thr | |
| NM_001257965.2:c.3050T>C | NP_001244894.1:p.Met1017Thr | |
| NR_047563.2:n.3075T>C | ||
| NR_047564.2:n.3283T>C | ||
| NM_001257966.2:c.2129-615T>C | NP_001244895.1:n.2129-615T>C |