Linked Data
ClinVar Variation Id:
2942371
ClinVar RCV Id:
RCV003805585
dbSNP Id:
rs1403926619
gnomAD v2:
8-94770728-T-C
gnomAD v3:
8-93758500-T-C
gnomAD v4:
8-93758500-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.93758500T>C , CM000670.2:g.93758500T>C | GRCh38 |
| NC_000008.10:g.94770728T>C , CM000670.1:g.94770728T>C | GRCh37 |
| NC_000008.9:g.94839904T>C | NCBI36 |
| NG_009190.1:g.8657T>C , LRG_688:g.8657T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323130.8:c.330T>C | ENSP00000314488.4:p.Asp110= | |
| ENST00000409623.8:c.330T>C | ENSP00000386966.4:p.Asp110= | |
| ENST00000452276.6:c.330T>C | ENSP00000388671.2:p.Asp110= | |
| ENST00000453906.6:c.330T>C | ENSP00000403035.2:p.Asp110= | |
| ENST00000520680.2:c.330T>C | ENSP00000428785.2:p.Asp110= | |
| ENST00000521065.2:c.330T>C | ENSP00000427947.2:p.Asp110= | |
| ENST00000521517.6:c.330T>C | ENSP00000430740.2:p.Asp110= | |
| ENST00000681998.1:c.330T>C | ENSP00000506773.1:p.Asp110= | |
| ENST00000682036.1:c.330T>C | ENSP00000508390.1:p.Asp110= | |
| ENST00000682577.1:c.330T>C | ENSP00000506963.1:p.Asp110= | |
| ENST00000682624.1:c.241T>C | ENSP00000508343.1:p.Trp81Arg | |
| ENST00000682700.1:c.330T>C | ENSP00000507627.1:p.Asp110= | |
| ENST00000682804.1:n.223T>C | ||
| ENST00000682837.1:c.330T>C | ENSP00000507920.1:p.Asp110= | |
| ENST00000682935.1:n.330T>C | ||
| ENST00000682984.1:c.312+2634T>C | ENSP00000507209.1:n.312+2634T>C | |
| ENST00000683078.1:c.330T>C | ENSP00000506796.1:p.Asp110= | |
| ENST00000683223.1:c.241T>C | ENSP00000507685.1:p.Trp81Arg | |
| ENST00000683238.1:n.151T>C | ||
| ENST00000683249.1:n.351T>C | ||
| ENST00000683336.1:c.330T>C | ENSP00000507695.1:p.Asp110= | |
| ENST00000683362.1:c.312+2634T>C | ENSP00000506985.1:n.312+2634T>C | |
| ENST00000683850.1:n.253T>C | ||
| ENST00000683919.1:c.330T>C | ENSP00000507617.1:p.Asp110= | |
| ENST00000683953.1:c.241T>C | ENSP00000508375.1:p.Trp81Arg | |
| ENST00000684023.1:c.330T>C | ENSP00000507461.1:p.Asp110= | |
| ENST00000684064.1:c.21T>C | ENSP00000508192.1:p.Asp7= | |
| ENST00000684089.1:n.320T>C | ||
| ENST00000684149.1:c.330T>C | ENSP00000507943.1:p.Asp110= | |
| ENST00000684416.1:n.155T>C | ||
| ENST00000684540.1:c.330T>C | ENSP00000507987.1:p.Asp110= | |
| ENST00000684733.1:n.265T>C | ||
| ENST00000453321.8:c.330T>C MANE Select | ENSP00000389998.3:p.Asp110= | |
| ENST00000323130.7:c.300T>C | ENSP00000314488.3:p.Asp100= | |
| ENST00000409623.7:c.-48T>C | ENSP00000386966.3:n.-48T>C | |
| ENST00000452276.5:c.21T>C | ENSP00000388671.1:p.Asp7= | |
| ENST00000453321.7:c.330T>C | ENSP00000389998.3:p.Asp110= | |
| ENST00000453906.5:c.330T>C | ENSP00000403035.1:p.Asp110= | |
| ENST00000455946.5:c.330T>C | ENSP00000416339.1:p.Asp110= | |
| ENST00000474944.5:n.350T>C | ||
| ENST00000475305.1:n.339T>C | ||
| ENST00000498673.5:c.-151T>C | ENSP00000430232.1:n.-151T>C | |
| ENST00000518319.5:c.-190T>C | ENSP00000430289.1:n.-190T>C | |
| ENST00000521065.1:c.236T>C | ||
| ENST00000521222.5:c.326T>C | ENSP00000429925.1:p.Met109Thr | |
| ENST00000521517.5:c.322T>C | ||
| NM_001142301.1:c.-48T>C , LRG_688t2:c.-48T>C | NP_001135773.1:n.-48T>C | |
| NM_153704.5:c.330T>C , LRG_688t1:c.330T>C | NP_714915.3:p.Asp110= | |
| NR_024522.1:n.401T>C | ||
| XM_006716686.2:c.27T>C | XP_006716749.1:p.Asp9= | |
| XM_011517363.1:c.330T>C | XP_011515665.1:p.Asp110= | |
| XR_428387.1:n.388T>C | ||
| XR_928360.1:n.388T>C | ||
| XR_928361.1:n.388T>C | ||
| XR_928362.1:n.388T>C | ||
| XM_006716686.4:c.27T>C | XP_006716749.1:p.Asp9= | |
| XM_011517363.3:c.330T>C | XP_011515665.1:p.Asp110= | |
| XM_024447326.1:c.-80T>C | XP_024303094.1:n.-80T>C | |
| XR_001745619.2:n.371T>C | ||
| XR_428387.2:n.371T>C | ||
| XR_928360.3:n.371T>C | ||
| XR_928362.3:n.371T>C | ||
| NM_153704.6:c.330T>C MANE Select | NP_714915.3:p.Asp110= | |
| NR_024522.2:n.351T>C |