Linked Data
ClinVar Variation Id:
137839
ClinVar RCV Id:
RCV000154988
RCV000266819
RCV000303282
RCV000306728
RCV000263263
RCV000357808
RCV000472153
RCV000769066
dbSNP Id:
rs145204073
ExAC:
2:179593804 T / C
gnomAD v2:
2-179593804-T-C
gnomAD v3:
2-178729077-T-C
gnomAD v4:
2-178729077-T-C
MyVariant Identifiers:
chr2:g.179593804T>C (hg19)
chr2:g.179593804_179593807delinsCAGG (hg19)
chr2:g.178729077T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178729077T>C , CM000664.2:g.178729077T>C | GRCh38 |
| NC_000002.11:g.179593804T>C , CM000664.1:g.179593804T>C | GRCh37 |
| NC_000002.10:g.179302049T>C | NCBI36 |
| NG_011618.3:g.106726A>G , LRG_391:g.106726A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.15229A>G | ENSP00000343764.6:p.Ile5077Val | |
| ENST00000342175.11:c.13858+9005A>G | ENSP00000340554.6:n.13858+9005A>G | |
| ENST00000359218.10:c.13657+9005A>G | ENSP00000352154.5:n.13657+9005A>G | |
| ENST00000342175.10:c.13858+9005A>G | ENSP00000340554.6:n.13858+9005A>G | |
| ENST00000342992.10:c.15229A>G | ENSP00000343764.6:p.Ile5077Val | |
| ENST00000359218.9:c.13657+9005A>G | ENSP00000352154.5:n.13657+9005A>G | |
| ENST00000460472.6:c.13282+9005A>G | ENSP00000434586.1:n.13282+9005A>G | |
| ENST00000589042.5:c.18961A>G MANE Select | ENSP00000467141.1:p.Ile6321Val | |
| ENST00000591111.5:c.18010A>G | ENSP00000465570.1:p.Ile6004Val | |
| ENST00000615779.4:c.18010A>G | ENSP00000483597.1:p.Ile6004Val | |
| NM_001256850.1:c.18010A>G | NP_001243779.1:p.Ile6004Val | |
| NM_001267550.2:c.18961A>G MANE Select | NP_001254479.2:p.Ile6321Val | |
| NM_003319.4:c.13282+9005A>G | NP_003310.4:n.13282+9005A>G | |
| NM_133378.4:c.15229A>G | NP_596869.4:p.Ile5077Val | |
| NM_133432.3:c.13657+9005A>G | NP_597676.3:n.13657+9005A>G | |
| NM_133437.4:c.13858+9005A>G | NP_597681.4:n.13858+9005A>G | |
| XM_011511729.1:c.18058A>G | XP_011510031.1:p.Ile6020Val | |
| XM_011511730.1:c.13468+9005A>G | XP_011510032.1:n.13468+9005A>G | |
| XM_011511731.1:c.13327+9005A>G | XP_011510033.1:n.13327+9005A>G | |
| XM_017004819.1:c.18013A>G | XP_016860308.1:p.Ile6005Val | |
| XM_017004820.1:c.15232A>G | XP_016860309.1:p.Ile5078Val | |
| XM_017004821.1:c.15229A>G | XP_016860310.1:p.Ile5077Val | |
| XM_017004822.1:c.18013A>G | XP_016860311.1:p.Ile6005Val | |
| XM_017004823.1:c.13423+9005A>G | XP_016860312.1:n.13423+9005A>G | |
| XM_024453094.1:c.18013A>G | XP_024308862.1:p.Ile6005Val | |
| XM_024453095.1:c.18013A>G | XP_024308863.1:p.Ile6005Val | |
| XM_024453096.1:c.18013A>G | XP_024308864.1:p.Ile6005Val | |
| XM_024453097.1:c.18013A>G | XP_024308865.1:p.Ile6005Val | |
| XM_024453098.1:c.18013A>G | XP_024308866.1:p.Ile6005Val | |
| XM_024453099.1:c.13423+9005A>G | XP_024308867.1:n.13423+9005A>G |