Linked Data
ClinVar Variation Id:
90682
ClinVar RCV Id:
RCV000076178
RCV000165088
RCV000412350
RCV000486935
RCV000524345
RCV000781557
RCV001030703
RCV001354505
RCV003153355
RCV002513806
dbSNP Id:
rs56170584
ExAC:
2:47630344 C / A
gnomAD v2:
2-47630344-C-A
gnomAD v3:
2-47403205-C-A
gnomAD v4:
2-47403205-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47403205C>A , CM000664.2:g.47403205C>A | GRCh38 |
| NC_000002.11:g.47630344C>A , CM000664.1:g.47630344C>A | GRCh37 |
| NC_000002.10:g.47483848C>A | NCBI36 |
| NG_007110.2:g.5082C>A , LRG_218:g.5082C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644900.2:c.14C>A | ENSP00000495641.2:p.Pro5Gln | |
| ENST00000233146.7:c.14C>A MANE Select | ENSP00000233146.2:p.Pro5Gln | |
| ENST00000543555.6:c.-31+30C>A | ENSP00000442697.1:n.-31+30C>A | |
| ENST00000644092.1:c.14C>A | ENSP00000496351.1:p.Pro5Gln | |
| ENST00000645339.1:c.14C>A | ENSP00000496441.1:p.Pro5Gln | |
| ENST00000645506.1:c.14C>A | ENSP00000495455.1:p.Pro5Gln | |
| ENST00000646415.1:c.14C>A | ENSP00000495543.1:p.Pro5Gln | |
| ENST00000233146.6:c.14C>A | ENSP00000233146.2:p.Pro5Gln | |
| ENST00000406134.5:c.14C>A | ENSP00000384199.1:p.Pro5Gln | |
| ENST00000454849.5:c.-31+30C>A | ENSP00000411482.1:n.-31+30C>A | |
| ENST00000543555.5:c.-31+30C>A | ENSP00000442697.1:n.-31+30C>A | |
| ENST00000610696.4:c.14C>A | ENSP00000483159.1:p.Pro5Gln | |
| ENST00000613514.4:c.14C>A | ENSP00000484137.1:p.Pro5Gln | |
| ENST00000617333.3:c.14C>A | ENSP00000482468.1:p.Pro5Gln | |
| ENST00000617938.4:c.14C>A | ENSP00000481158.1:p.Pro5Gln | |
| ENST00000621359.2:c.14C>A | ENSP00000481416.1:p.Pro5Gln | |
| NM_000251.2:c.14C>A , LRG_218t1:c.14C>A | NP_000242.1:p.Pro5Gln | |
| NM_001258281.1:c.-31+30C>A | NP_001245210.1:n.-31+30C>A | |
| XM_005264332.2:c.14C>A | XP_005264389.2:p.Pro5Gln | |
| XM_011532867.1:c.14C>A | XP_011531169.1:p.Pro5Gln | |
| XR_939685.1:n.86C>A | ||
| XM_005264332.4:c.14C>A | XP_005264389.2:p.Pro5Gln | |
| XM_011532867.2:c.14C>A | XP_011531169.1:p.Pro5Gln | |
| XR_001738747.2:n.76C>A | ||
| XR_939685.2:n.76C>A | ||
| NM_000251.3:c.14C>A MANE Select | NP_000242.1:p.Pro5Gln |