Linked Data
ClinVar Variation Id:
158716
ClinVar RCV Id:
RCV000146153
dbSNP Id:
rs587783682
gnomAD v2:
12-49427198-G-A
gnomAD v4:
12-49033415-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49033415G>A , CM000674.2:g.49033415G>A | GRCh38 |
| NC_000012.11:g.49427198G>A , CM000674.1:g.49427198G>A | GRCh37 |
| NC_000012.10:g.47713465G>A | NCBI36 |
| NG_027827.1:g.26910C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683543.2:c.11290C>T | ENSP00000506726.1:p.Gln3764Ter | |
| ENST00000685166.1:c.11299C>T | ENSP00000509386.1:p.Gln3767Ter | |
| ENST00000685554.1:c.850C>T | ENSP00000508640.1:p.Gln284Ter | |
| ENST00000687201.1:c.2869C>T | ENSP00000510037.1:p.Gln957Ter | |
| ENST00000692637.1:c.11287C>T | ENSP00000509666.1:p.Gln3763Ter | |
| ENST00000692841.1:c.2769C>T | ENSP00000508711.1:n.2769C>T | |
| ENST00000301067.12:c.11290C>T MANE Select | ENSP00000301067.7:p.Gln3764Ter | |
| ENST00000301067.11:c.11290C>T | ENSP00000301067.7:p.Gln3764Ter | |
| NM_003482.3:c.11290C>T | NP_003473.3:p.Gln3764Ter | |
| XM_005269162.3:c.11290C>T | XP_005269219.1:p.Gln3764Ter | |
| XM_006719614.2:c.11299C>T | XP_006719677.1:p.Gln3767Ter | |
| XM_006719616.2:c.11287C>T | XP_006719679.1:p.Gln3763Ter | |
| XM_011538770.1:c.11299C>T | XP_011537072.1:p.Gln3767Ter | |
| XM_011538771.1:c.11296C>T | XP_011537073.1:p.Gln3766Ter | |
| XM_011538772.1:c.11290C>T | XP_011537074.1:p.Gln3764Ter | |
| XM_011538773.1:c.11287C>T | XP_011537075.1:p.Gln3763Ter | |
| XM_011538774.1:c.11278C>T | XP_011537076.1:p.Gln3760Ter | |
| XM_011538775.1:c.11299C>T | XP_011537077.1:p.Gln3767Ter | |
| XM_011538776.1:c.11206C>T | XP_011537078.1:p.Gln3736Ter | |
| XR_944740.1:n.13619C>T | ||
| XM_005269162.4:c.11290C>T | XP_005269219.1:p.Gln3764Ter | |
| XM_006719614.4:c.11299C>T | XP_006719677.1:p.Gln3767Ter | |
| XM_006719616.3:c.11287C>T | XP_006719679.1:p.Gln3763Ter | |
| XM_011538770.2:c.11299C>T | XP_011537072.1:p.Gln3767Ter | |
| XM_011538771.2:c.11296C>T | XP_011537073.1:p.Gln3766Ter | |
| XM_011538772.2:c.11290C>T | XP_011537074.1:p.Gln3764Ter | |
| XM_011538773.2:c.11287C>T | XP_011537075.1:p.Gln3763Ter | |
| XM_011538774.2:c.11278C>T | XP_011537076.1:p.Gln3760Ter | |
| XM_011538776.2:c.11206C>T | XP_011537078.1:p.Gln3736Ter | |
| XR_001748874.1:n.12608C>T | ||
| NM_003482.4:c.11290C>T MANE Select | NP_003473.3:p.Gln3764Ter |