Linked Data
ClinVar Variation Id:
1515499
ClinVar RCV Id:
RCV002021141
dbSNP Id:
rs757192472
ExAC:
X:32482812 T / C
gnomAD v2:
X-32482812-T-C
gnomAD v4:
X-32464695-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32464695T>C , CM000685.2:g.32464695T>C | GRCh38 |
| NC_000023.10:g.32482812T>C , CM000685.1:g.32482812T>C | GRCh37 |
| NC_000023.9:g.32392733T>C | NCBI36 |
| NG_012232.1:g.879915A>G , LRG_199:g.879915A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682899.1:n.3374A>G | ||
| ENST00000357033.9:c.3167A>G MANE Select | ENSP00000354923.3:p.His1056Arg | |
| ENST00000357033.8:c.3167A>G | ENSP00000354923.3:p.His1056Arg | |
| ENST00000378677.6:c.3155A>G | ENSP00000367948.2:p.His1052Arg | |
| ENST00000420596.5:c.94-99496A>G | ENSP00000399897.1:n.94-99496A>G | |
| ENST00000448370.5:c.94-99985A>G | ENSP00000388559.1:n.94-99985A>G | |
| ENST00000488902.5:n.336-247632A>G | ||
| ENST00000619831.4:c.3155A>G | ENSP00000479270.1:p.His1052Arg | |
| ENST00000620040.4:c.3167A>G | ENSP00000478150.1:p.His1056Arg | |
| NM_000109.3:c.3143A>G | NP_000100.2:p.His1048Arg | |
| NM_004006.2:c.3167A>G , LRG_199t1:c.3167A>G | NP_003997.1:p.His1056Arg | |
| NM_004009.3:c.3155A>G | NP_004000.1:p.His1052Arg | |
| NM_004010.3:c.2798A>G | NP_004001.1:p.His933Arg | |
| XM_006724468.2:c.3167A>G | XP_006724531.1:p.His1056Arg | |
| XM_006724469.2:c.3143A>G | XP_006724532.1:p.His1048Arg | |
| XM_006724470.2:c.3167A>G | XP_006724533.1:p.His1056Arg | |
| XM_006724471.2:c.3167A>G | XP_006724534.1:p.His1056Arg | |
| XM_006724472.2:c.3038A>G | XP_006724535.1:p.His1013Arg | |
| XM_006724473.2:c.3167A>G | XP_006724536.1:p.His1056Arg | |
| XM_006724474.2:c.3167A>G | XP_006724537.1:p.His1056Arg | |
| XM_006724475.2:c.3167A>G | XP_006724538.1:p.His1056Arg | |
| XM_011545467.1:c.3167A>G | XP_011543769.1:p.His1056Arg | |
| XM_011545468.1:c.3167A>G | XP_011543770.1:p.His1056Arg | |
| XM_011545469.1:c.3167A>G | XP_011543771.1:p.His1056Arg | |
| XM_006724469.3:c.3143A>G | XP_006724532.1:p.His1048Arg | |
| XM_006724470.3:c.3167A>G | XP_006724533.1:p.His1056Arg | |
| XM_006724474.3:c.3167A>G | XP_006724537.1:p.His1056Arg | |
| XM_011545468.2:c.3167A>G | XP_011543770.1:p.His1056Arg | |
| XM_017029328.1:c.3167A>G | XP_016884817.1:p.His1056Arg | |
| XM_017029329.1:c.3167A>G | XP_016884818.1:p.His1056Arg | |
| XM_017029330.2:c.3167A>G | XP_016884819.1:p.His1056Arg | |
| NM_000109.4:c.3143A>G | NP_000100.3:p.His1048Arg | |
| NM_004006.3:c.3167A>G MANE Select | NP_003997.2:p.His1056Arg |