Linked Data
ClinVar Variation Id:
199030
dbSNP Id:
rs781811015
ExAC:
X:76937683 C / T
gnomAD v2:
X-76937683-C-T
gnomAD v3:
X-77682191-C-T
gnomAD v4:
X-77682191-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.77682191C>T , CM000685.2:g.77682191C>T | GRCh38 |
| NC_000023.10:g.76937683C>T , CM000685.1:g.76937683C>T | GRCh37 |
| NC_000023.9:g.76824339C>T | NCBI36 |
| NG_008838.2:g.109031G>A | |
| NG_008838.3:g.109079G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373344.11:c.3065G>A MANE Select | ENSP00000362441.4:p.Arg1022Gln | |
| ENST00000373344.9:c.3065G>A | ENSP00000362441.4:p.Arg1022Gln | |
| ENST00000395603.7:c.2951G>A | ENSP00000378967.3:p.Arg984Gln | |
| ENST00000480283.5:c.*2693G>A | ENSP00000480196.1:n.*2693G>A | |
| ENST00000624166.3:c.2861G>A | ENSP00000485103.1:p.Arg954Gln | |
| NM_000489.4:c.3065G>A | NP_000480.3:p.Arg1022Gln | |
| NM_138270.3:c.2951G>A | NP_612114.2:p.Arg984Gln | |
| XM_005262153.3:c.3062G>A | XP_005262210.2:p.Arg1021Gln | |
| XM_005262154.3:c.2978G>A | XP_005262211.2:p.Arg993Gln | |
| XM_005262155.3:c.2948G>A | XP_005262212.2:p.Arg983Gln | |
| XM_005262156.3:c.2900G>A | XP_005262213.2:p.Arg967Gln | |
| XM_005262157.3:c.2861G>A | XP_005262214.2:p.Arg954Gln | |
| XM_006724666.2:c.2948G>A | XP_006724729.1:p.Arg983Gln | |
| XM_006724667.2:c.2786G>A | XP_006724730.1:p.Arg929Gln | |
| XM_006724668.2:c.3065G>A | XP_006724731.1:p.Arg1022Gln | |
| XR_938400.1:n.3333G>A | ||
| NM_000489.5:c.3065G>A | NP_000480.3:p.Arg1022Gln | |
| XM_005262153.5:c.3062G>A | XP_005262210.2:p.Arg1021Gln | |
| XM_005262154.5:c.2978G>A | XP_005262211.2:p.Arg993Gln | |
| XM_005262155.4:c.2948G>A | XP_005262212.2:p.Arg983Gln | |
| XM_005262156.4:c.2900G>A | XP_005262213.2:p.Arg967Gln | |
| XM_005262157.5:c.2861G>A | XP_005262214.2:p.Arg954Gln | |
| XM_006724666.4:c.2948G>A | XP_006724729.1:p.Arg983Gln | |
| XM_006724667.3:c.2786G>A | XP_006724730.1:p.Arg929Gln | |
| XM_006724668.3:c.3065G>A | XP_006724731.1:p.Arg1022Gln | |
| XM_017029601.2:c.2975G>A | XP_016885090.1:p.Arg992Gln | |
| XM_017029602.1:c.2945G>A | XP_016885091.1:p.Arg982Gln | |
| XM_017029603.1:c.2897G>A | XP_016885092.1:p.Arg966Gln | |
| XM_017029604.2:c.2864G>A | XP_016885093.1:p.Arg955Gln | |
| XM_017029605.1:c.2861G>A | XP_016885094.1:p.Arg954Gln | |
| XM_017029606.2:c.2834G>A | XP_016885095.1:p.Arg945Gln | |
| XM_017029607.2:c.2831G>A | XP_016885096.1:p.Arg944Gln | |
| XM_017029608.2:c.2783G>A | XP_016885097.1:p.Arg928Gln | |
| XM_017029609.1:c.2747G>A | XP_016885098.1:p.Arg916Gln | |
| XM_017029610.1:c.2744G>A | XP_016885099.1:p.Arg915Gln | |
| XM_017029611.1:c.2699G>A | XP_016885100.1:p.Arg900Gln | |
| XR_001755700.2:n.3290G>A | ||
| NM_138270.4:c.2951G>A | NP_612114.2:p.Arg984Gln | |
| NM_000489.6:c.3065G>A MANE Select | NP_000480.3:p.Arg1022Gln | |
| NM_138270.5:c.2951G>A | NP_612114.2:p.Arg984Gln |