Linked Data
ClinVar Variation Id:
1385314
ClinVar RCV Id:
RCV001902853
dbSNP Id:
rs774863206
gnomAD v4:
11-68047740-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68047740C>A , CM000673.2:g.68047740C>A | GRCh38 |
| NC_000011.9:g.67815207C>A , CM000673.1:g.67815207C>A | GRCh37 |
| NC_000011.8:g.67571783C>A | NCBI36 |
| NG_007878.1:g.13725C>A , LRG_115:g.13725C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530449.2:n.24C>A | ||
| ENST00000698254.1:c.928C>A | ENSP00000513629.1:p.Arg310Ser | |
| ENST00000698255.1:c.1348C>A | ENSP00000513630.1:p.Arg450Ser | |
| ENST00000698256.1:c.865C>A | ||
| ENST00000698257.1:n.817C>A | ||
| ENST00000698258.1:n.457C>A | ||
| ENST00000698259.1:n.223C>A | ||
| ENST00000265686.8:c.1399C>A MANE Select | ENSP00000265686.3:p.Arg467Ser | |
| ENST00000265686.7:c.1399C>A | ENSP00000265686.3:p.Arg467Ser | |
| ENST00000525516.1:n.193C>A | ||
| ENST00000525724.5:n.711C>A | ||
| ENST00000528981.5:c.551C>A | ||
| ENST00000529364.1:c.810C>A | ||
| ENST00000532635.5:c.751C>A | ENSP00000434407.1:p.Arg251Ser | |
| ENST00000533005.5:n.435C>A | ||
| NM_006019.3:c.1399C>A | NP_006010.2:p.Arg467Ser | |
| NM_006053.3:c.751C>A | NP_006044.1:p.Arg251Ser | |
| XM_005273709.2:c.1399C>A | XP_005273766.1:p.Arg467Ser | |
| XM_011544726.1:c.1399C>A | XP_011543028.1:p.Arg467Ser | |
| XM_011544727.1:c.1399C>A | XP_011543029.1:p.Arg467Ser | |
| XM_011544728.1:c.1399C>A | XP_011543030.1:p.Arg467Ser | |
| XM_011544729.1:c.1415C>A | XP_011543031.1:p.Ser472Ter | |
| XR_949754.1:n.1403C>A | ||
| NM_001351059.1:c.505C>A | NP_001337988.1:p.Arg169Ser | |
| XM_024448320.1:c.1415C>A | XP_024304088.1:p.Ser472Ter | |
| XM_024448321.1:c.1415C>A | XP_024304089.1:p.Ser472Ter | |
| XM_024448322.1:c.1415C>A | XP_024304090.1:p.Ser472Ter | |
| XM_024448323.1:c.1415C>A | XP_024304091.1:p.Ser472Ter | |
| XM_024448324.1:c.1415C>A | XP_024304092.1:p.Ser472Ter | |
| XR_001747721.2:n.1523C>A | ||
| XR_001747722.1:n.1536C>A | ||
| XR_001747723.2:n.1536C>A | ||
| XR_002957115.1:n.1537C>A | ||
| NM_006019.4:c.1399C>A MANE Select | NP_006010.2:p.Arg467Ser | |
| NM_001351059.2:c.505C>A | NP_001337988.1:p.Arg169Ser | |
| NM_006053.4:c.751C>A | NP_006044.1:p.Arg251Ser |