Linked Data
ClinVar Variation Id:
286670
dbSNP Id:
rs782058125
ExAC:
X:76939822 T / C
gnomAD v2:
X-76939822-T-C
gnomAD v4:
X-77684330-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.77684330T>C , CM000685.2:g.77684330T>C | GRCh38 |
| NC_000023.10:g.76939822T>C , CM000685.1:g.76939822T>C | GRCh37 |
| NC_000023.9:g.76826478T>C | NCBI36 |
| NG_008838.2:g.106892A>G | |
| NG_008838.3:g.106940A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373344.11:c.926A>G MANE Select | ENSP00000362441.4:p.Tyr309Cys | |
| ENST00000373344.9:c.926A>G | ENSP00000362441.4:p.Tyr309Cys | |
| ENST00000395603.7:c.812A>G | ENSP00000378967.3:p.Tyr271Cys | |
| ENST00000480283.5:c.*554A>G | ENSP00000480196.1:n.*554A>G | |
| ENST00000623321.3:c.761A>G | ENSP00000485127.1:p.Tyr254Cys | |
| ENST00000624032.3:c.926A>G | ENSP00000485253.1:p.Tyr309Cys | |
| ENST00000624166.3:c.809A>G | ENSP00000485103.1:p.Tyr270Cys | |
| NM_000489.4:c.926A>G | NP_000480.3:p.Tyr309Cys | |
| NM_138270.3:c.812A>G | NP_612114.2:p.Tyr271Cys | |
| XM_005262153.3:c.923A>G | XP_005262210.2:p.Tyr308Cys | |
| XM_005262154.3:c.926A>G | XP_005262211.2:p.Tyr309Cys | |
| XM_005262155.3:c.809A>G | XP_005262212.2:p.Tyr270Cys | |
| XM_005262156.3:c.761A>G | XP_005262213.2:p.Tyr254Cys | |
| XM_005262157.3:c.809A>G | XP_005262214.2:p.Tyr270Cys | |
| XM_006724666.2:c.809A>G | XP_006724729.1:p.Tyr270Cys | |
| XM_006724667.2:c.647A>G | XP_006724730.1:p.Tyr216Cys | |
| XM_006724668.2:c.926A>G | XP_006724731.1:p.Tyr309Cys | |
| XR_938400.1:n.1194A>G | ||
| NM_000489.5:c.926A>G | NP_000480.3:p.Tyr309Cys | |
| XM_005262153.5:c.923A>G | XP_005262210.2:p.Tyr308Cys | |
| XM_005262154.5:c.926A>G | XP_005262211.2:p.Tyr309Cys | |
| XM_005262155.4:c.809A>G | XP_005262212.2:p.Tyr270Cys | |
| XM_005262156.4:c.761A>G | XP_005262213.2:p.Tyr254Cys | |
| XM_005262157.5:c.809A>G | XP_005262214.2:p.Tyr270Cys | |
| XM_006724666.4:c.809A>G | XP_006724729.1:p.Tyr270Cys | |
| XM_006724667.3:c.647A>G | XP_006724730.1:p.Tyr216Cys | |
| XM_006724668.3:c.926A>G | XP_006724731.1:p.Tyr309Cys | |
| XM_017029601.2:c.923A>G | XP_016885090.1:p.Tyr308Cys | |
| XM_017029602.1:c.806A>G | XP_016885091.1:p.Tyr269Cys | |
| XM_017029603.1:c.758A>G | XP_016885092.1:p.Tyr253Cys | |
| XM_017029604.2:c.812A>G | XP_016885093.1:p.Tyr271Cys | |
| XM_017029605.1:c.809A>G | XP_016885094.1:p.Tyr270Cys | |
| XM_017029606.2:c.695A>G | XP_016885095.1:p.Tyr232Cys | |
| XM_017029607.2:c.692A>G | XP_016885096.1:p.Tyr231Cys | |
| XM_017029608.2:c.644A>G | XP_016885097.1:p.Tyr215Cys | |
| XM_017029609.1:c.695A>G | XP_016885098.1:p.Tyr232Cys | |
| XM_017029610.1:c.692A>G | XP_016885099.1:p.Tyr231Cys | |
| XM_017029611.1:c.647A>G | XP_016885100.1:p.Tyr216Cys | |
| XR_001755700.2:n.1151A>G | ||
| NM_138270.4:c.812A>G | NP_612114.2:p.Tyr271Cys | |
| NM_000489.6:c.926A>G MANE Select | NP_000480.3:p.Tyr309Cys | |
| NM_138270.5:c.812A>G | NP_612114.2:p.Tyr271Cys |