Linked Data
ClinVar Variation Id:
94702
ClinVar RCV Id:
RCV000723715
RCV001083222
RCV000853038
RCV001167894
RCV001835678
RCV002265600
RCV002354279
RCV004537361
dbSNP Id:
rs142807436
ExAC:
X:32235151 C / T
gnomAD v2:
X-32235151-C-T
gnomAD v3:
X-32217034-C-T
gnomAD v4:
X-32217034-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32217034C>T , CM000685.2:g.32217034C>T | GRCh38 |
| NC_000023.10:g.32235151C>T , CM000685.1:g.32235151C>T | GRCh37 |
| NC_000023.9:g.32145072C>T | NCBI36 |
| NG_012232.1:g.1127576G>A , LRG_199:g.1127576G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.1166G>A | ENSP00000350765.3:p.Arg389Gln | |
| ENST00000357033.9:c.6320G>A MANE Select | ENSP00000354923.3:p.Arg2107Gln | |
| ENST00000619831.5:c.2288G>A | ENSP00000479270.2:p.Arg763Gln | |
| ENST00000357033.8:c.6320G>A | ENSP00000354923.3:p.Arg2107Gln | |
| ENST00000378677.6:c.6308G>A | ENSP00000367948.2:p.Arg2103Gln | |
| ENST00000488902.5:n.365G>A | ||
| ENST00000619831.4:c.6308G>A | ENSP00000479270.1:p.Arg2103Gln | |
| ENST00000620040.4:c.6320G>A | ENSP00000478150.1:p.Arg2107Gln | |
| NM_000109.3:c.6296G>A | NP_000100.2:p.Arg2099Gln | |
| NM_004006.2:c.6320G>A , LRG_199t1:c.6320G>A | NP_003997.1:p.Arg2107Gln | |
| NM_004009.3:c.6308G>A | NP_004000.1:p.Arg2103Gln | |
| NM_004010.3:c.5951G>A | NP_004001.1:p.Arg1984Gln | |
| NM_004011.3:c.2297G>A | NP_004002.2:p.Arg766Gln | |
| NM_004012.3:c.2288G>A | NP_004003.1:p.Arg763Gln | |
| XM_006724468.2:c.6320G>A | XP_006724531.1:p.Arg2107Gln | |
| XM_006724469.2:c.6296G>A | XP_006724532.1:p.Arg2099Gln | |
| XM_006724470.2:c.6320G>A | XP_006724533.1:p.Arg2107Gln | |
| XM_006724471.2:c.6320G>A | XP_006724534.1:p.Arg2107Gln | |
| XM_006724472.2:c.6191G>A | XP_006724535.1:p.Arg2064Gln | |
| XM_006724473.2:c.6182G>A | XP_006724536.1:p.Arg2061Gln | |
| XM_006724474.2:c.6320G>A | XP_006724537.1:p.Arg2107Gln | |
| XM_006724475.2:c.6320G>A | XP_006724538.1:p.Arg2107Gln | |
| XM_011545467.1:c.6197G>A | XP_011543769.1:p.Arg2066Gln | |
| XM_011545468.1:c.6320G>A | XP_011543770.1:p.Arg2107Gln | |
| XM_006724469.3:c.6296G>A | XP_006724532.1:p.Arg2099Gln | |
| XM_006724470.3:c.6320G>A | XP_006724533.1:p.Arg2107Gln | |
| XM_006724474.3:c.6320G>A | XP_006724537.1:p.Arg2107Gln | |
| XM_011545468.2:c.6320G>A | XP_011543770.1:p.Arg2107Gln | |
| XM_017029328.1:c.6320G>A | XP_016884817.1:p.Arg2107Gln | |
| XM_017029329.1:c.6320G>A | XP_016884818.1:p.Arg2107Gln | |
| XM_017029330.2:c.6320G>A | XP_016884819.1:p.Arg2107Gln | |
| XM_017029331.1:c.494G>A | XP_016884820.1:p.Arg165Gln | |
| NM_000109.4:c.6296G>A | NP_000100.3:p.Arg2099Gln | |
| NM_004006.3:c.6320G>A MANE Select | NP_003997.2:p.Arg2107Gln | |
| NM_004011.4:c.2297G>A | NP_004002.3:p.Arg766Gln | |
| NM_004012.4:c.2288G>A | NP_004003.2:p.Arg763Gln |