Linked Data
ClinVar Variation Id:
342603
ClinVar RCV Id:
RCV000327367
dbSNP Id:
rs3732783
ExAC:
3:113890789 T / C
gnomAD v2:
3-113890789-T-C
gnomAD v3:
3-114171942-T-C
gnomAD v4:
3-114171942-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.114171942T>C , CM000665.2:g.114171942T>C | GRCh38 |
| NC_000003.11:g.113890789T>C , CM000665.1:g.113890789T>C | GRCh37 |
| NC_000003.10:g.115373479T>C | NCBI36 |
| NG_008842.2:g.32466A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698213.1:c.51A>G | ENSP00000513607.1:p.Ala17= | |
| ENST00000383673.5:c.51A>G MANE Select | ENSP00000373169.2:p.Ala17= | |
| ENST00000295881.9:c.51A>G | ENSP00000295881.6:p.Ala17= | |
| ENST00000383673.4:c.51A>G | ENSP00000373169.2:p.Ala17= | |
| ENST00000460779.5:c.51A>G | ENSP00000419402.1:p.Ala17= | |
| ENST00000467632.5:c.51A>G | ENSP00000420662.1:p.Ala17= | |
| NM_000796.5:c.51A>G | NP_000787.2:p.Ala17= | |
| NM_001282563.2:c.51A>G | NP_001269492.1:p.Ala17= | |
| NM_001290809.1:c.51A>G | NP_001277738.1:p.Ala17= | |
| NM_033663.5:c.51A>G | NP_387512.3:p.Ala17= | |
| XM_011512510.1:c.51A>G | XP_011510812.1:p.Ala17= | |
| XM_011512511.1:c.51A>G | XP_011510813.1:p.Ala17= | |
| XM_011512512.1:c.51A>G | XP_011510814.1:p.Ala17= | |
| XM_017005829.1:c.51A>G | XP_016861318.1:p.Ala17= | |
| NM_000796.6:c.51A>G MANE Select | NP_000787.2:p.Ala17= | |
| NM_033663.6:c.51A>G | NP_387512.3:p.Ala17= |