Linked Data
ClinVar Variation Id:
2175608
ClinVar RCV Id:
RCV002579356
MyVariant Identifiers:
chr3:g.49160745A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49123312A>G , CM000665.2:g.49123312A>G | GRCh38 |
| NC_000003.11:g.49160745A>G , CM000665.1:g.49160745A>G | GRCh37 |
| NC_000003.10:g.49135749A>G | NCBI36 |
| NG_008094.1:g.14855T>C | |
| NG_054716.1:g.2627T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305544.9:c.4044T>C MANE Select | ENSP00000307156.4:p.Asn1348= | |
| ENST00000305544.8:c.4044T>C | ENSP00000307156.4:p.Asn1348= | |
| ENST00000418109.5:c.4044T>C | ENSP00000388325.1:p.Asn1348= | |
| ENST00000469665.1:n.274T>C | ||
| NM_002292.3:c.4044T>C | NP_002283.3:p.Asn1348= | |
| XM_005265127.3:c.4044T>C | XP_005265184.1:p.Asn1348= | |
| XM_005265127.4:c.4044T>C | XP_005265184.1:p.Asn1348= | |
| NM_002292.4:c.4044T>C MANE Select | NP_002283.3:p.Asn1348= |