Linked Data
ClinVar Variation Id:
47843
dbSNP Id:
rs200204761
ExAC:
2:179603991 T / G
gnomAD v2:
2-179603991-T-G
gnomAD v3:
2-178739264-T-G
gnomAD v4:
2-178739264-T-G
PubMed:
PMID:23861362
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178739264T>G , CM000664.2:g.178739264T>G | GRCh38 |
| NC_000002.11:g.179603991T>G , CM000664.1:g.179603991T>G | GRCh37 |
| NC_000002.10:g.179312236T>G | NCBI36 |
| NG_011618.3:g.96539A>C , LRG_391:g.96539A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.10361-904A>C | ENSP00000343764.6:n.10361-904A>C | |
| ENST00000342175.11:c.13456A>C | ENSP00000340554.6:p.Asn4486His | |
| ENST00000359218.10:c.13255A>C | ENSP00000352154.5:p.Asn4419His | |
| ENST00000342175.10:c.13456A>C | ENSP00000340554.6:p.Asn4486His | |
| ENST00000342992.10:c.10361-904A>C | ENSP00000343764.6:n.10361-904A>C | |
| ENST00000359218.9:c.13255A>C | ENSP00000352154.5:p.Asn4419His | |
| ENST00000460472.6:c.12880A>C | ENSP00000434586.1:p.Asn4294His | |
| ENST00000589042.5:c.13969A>C MANE Select | ENSP00000467141.1:p.Asn4657His | |
| ENST00000591111.5:c.13018A>C | ENSP00000465570.1:p.Asn4340His | |
| ENST00000615779.4:c.13018A>C | ENSP00000483597.1:p.Asn4340His | |
| NM_001256850.1:c.13018A>C | NP_001243779.1:p.Asn4340His | |
| NM_001267550.2:c.13969A>C MANE Select | NP_001254479.2:p.Asn4657His | |
| NM_003319.4:c.12880A>C | NP_003310.4:p.Asn4294His | |
| NM_133378.4:c.10361-904A>C | NP_596869.4:n.10361-904A>C | |
| NM_133432.3:c.13255A>C | NP_597676.3:p.Asn4419His | |
| NM_133437.4:c.13456A>C | NP_597681.4:p.Asn4486His | |
| XM_011511729.1:c.13066A>C | XP_011510031.1:p.Asn4356His | |
| XM_011511730.1:c.13066A>C | XP_011510032.1:p.Asn4356His | |
| XM_011511731.1:c.12925A>C | XP_011510033.1:p.Asn4309His | |
| XM_017004819.1:c.13021A>C | XP_016860308.1:p.Asn4341His | |
| XM_017004820.1:c.10364-904A>C | XP_016860309.1:n.10364-904A>C | |
| XM_017004821.1:c.10361-904A>C | XP_016860310.1:n.10361-904A>C | |
| XM_017004822.1:c.13021A>C | XP_016860311.1:p.Asn4341His | |
| XM_017004823.1:c.13021A>C | XP_016860312.1:p.Asn4341His | |
| XM_024453094.1:c.13021A>C | XP_024308862.1:p.Asn4341His | |
| XM_024453095.1:c.13021A>C | XP_024308863.1:p.Asn4341His | |
| XM_024453096.1:c.13021A>C | XP_024308864.1:p.Asn4341His | |
| XM_024453097.1:c.13021A>C | XP_024308865.1:p.Asn4341His | |
| XM_024453098.1:c.13021A>C | XP_024308866.1:p.Asn4341His | |
| XM_024453099.1:c.13021A>C | XP_024308867.1:p.Asn4341His |