Linked Data
ClinVar Variation Id:
1297642
ClinVar RCV Id:
RCV001723410
dbSNP Id:
rs2138843742
gnomAD v4:
14-30878830-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.30878830G>T , CM000676.2:g.30878830G>T | GRCh38 |
| NC_000014.8:g.31348036G>T , CM000676.1:g.31348036G>T | GRCh37 |
| NC_000014.7:g.30417787G>T | NCBI36 |
| NG_008211.2:g.9296G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216361.9:c.454G>T | ENSP00000216361.5:p.Gly152Trp | |
| ENST00000396618.9:c.259G>T MANE Select | ENSP00000379862.3:p.Gly87Trp | |
| ENST00000555117.2:c.259G>T | ENSP00000493569.1:p.Gly87Trp | |
| ENST00000643575.1:c.259G>T | ENSP00000494838.1:p.Gly87Trp | |
| ENST00000643697.1:n.504G>T | ||
| ENST00000644874.2:c.259G>T | ENSP00000496360.1:p.Gly87Trp | |
| ENST00000216361.8:c.259G>T | ENSP00000216361.4:p.Gly87Trp | |
| ENST00000396618.7:c.259G>T | ENSP00000379862.3:p.Gly87Trp | |
| ENST00000460581.6:c.-78G>T | ENSP00000451713.1:n.-78G>T | |
| ENST00000475087.5:c.259G>T | ENSP00000451528.1:p.Gly87Trp | |
| ENST00000553772.5:c.239+1102G>T | ENSP00000452343.1:n.239+1102G>T | |
| ENST00000553833.5:n.413G>T | ||
| ENST00000555881.5:c.83-1622G>T | ENSP00000452569.1:n.83-1622G>T | |
| ENST00000556908.5:c.211G>T | ENSP00000452541.1:p.Gly71Trp | |
| ENST00000557065.1:c.156-593G>T | ENSP00000451629.1:n.156-593G>T | |
| NM_001135058.1:c.259G>T | NP_001128530.1:p.Gly87Trp | |
| NM_004086.2:c.259G>T | NP_004077.1:p.Gly87Trp | |
| NR_038356.1:n.1618-2278C>A | ||
| XM_011536539.1:c.259G>T | XP_011534841.1:p.Gly87Trp | |
| NM_001347720.1:c.454G>T | NP_001334649.1:p.Gly152Trp | |
| XM_017021071.1:c.454G>T | XP_016876560.1:p.Gly152Trp | |
| XM_024449506.1:c.259G>T | XP_024305274.1:p.Gly87Trp | |
| NM_004086.3:c.259G>T MANE Select | NP_004077.1:p.Gly87Trp | |
| NM_001135058.2:c.259G>T | NP_001128530.1:p.Gly87Trp | |
| NM_001347720.2:c.454G>T | NP_001334649.1:p.Gly152Trp |