Linked Data
ClinVar Variation Id:
162576
ClinVar RCV Id:
RCV000712184
RCV000764624
RCV000550298
RCV001156479
RCV001270116
RCV001252051
RCV004532672
dbSNP Id:
rs34505698
ExAC:
6:129635920 G / A
gnomAD v2:
6-129635920-G-A
gnomAD v3:
6-129314775-G-A
gnomAD v4:
6-129314775-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129314775G>A , CM000668.2:g.129314775G>A | GRCh38 |
| NC_000006.11:g.129635920G>A , CM000668.1:g.129635920G>A | GRCh37 |
| NC_000006.10:g.129677613G>A | NCBI36 |
| NG_008678.1:g.436635G>A , LRG_409:g.436635G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617695.5:c.3532G>A | ENSP00000481744.2:p.Ala1178Thr | |
| ENST00000618192.5:c.3796G>A | ENSP00000480802.2:p.Ala1266Thr | |
| ENST00000421865.3:c.3532G>A MANE Select | ENSP00000400365.2:p.Ala1178Thr | |
| ENST00000421865.2:c.3532G>A | ENSP00000400365.2:p.Ala1178Thr | |
| ENST00000617695.4:c.3532G>A | ENSP00000481744.1:p.Ala1178Thr | |
| ENST00000618192.4:c.3532G>A | ENSP00000480802.1:p.Ala1178Thr | |
| NM_000426.3:c.3532G>A , LRG_409t1:c.3532G>A | NP_000417.2:p.Ala1178Thr | |
| NM_001079823.1:c.3532G>A | NP_001073291.1:p.Ala1178Thr | |
| XM_005266981.2:c.3796G>A | XP_005267038.1:p.Ala1266Thr | |
| XM_005266982.2:c.3796G>A | XP_005267039.1:p.Ala1266Thr | |
| XM_011535820.1:c.3796G>A | XP_011534122.1:p.Ala1266Thr | |
| XM_005266981.3:c.3796G>A | XP_005267038.1:p.Ala1266Thr | |
| XM_005266982.3:c.3796G>A | XP_005267039.1:p.Ala1266Thr | |
| XM_011535820.2:c.3796G>A | XP_011534122.1:p.Ala1266Thr | |
| XM_017010851.2:c.3802G>A | XP_016866340.1:p.Ala1268Thr | |
| XM_017010852.1:c.1927G>A | XP_016866341.1:p.Ala643Thr | |
| XM_017010853.1:c.3796G>A | XP_016866342.1:p.Ala1266Thr | |
| NM_000426.4:c.3532G>A MANE Select | NP_000417.3:p.Ala1178Thr | |
| NM_001079823.2:c.3532G>A | NP_001073291.2:p.Ala1178Thr |