Linked Data
ClinVar Variation Id:
134076
dbSNP Id:
rs546886845
ExAC:
17:37863262 G / T
gnomAD v2:
17-37863262-G-T
gnomAD v3:
17-39707009-G-T
gnomAD v4:
17-39707009-G-T
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39707009G>T , CM000679.2:g.39707009G>T | GRCh38 |
| NC_000017.10:g.37863262G>T , CM000679.1:g.37863262G>T | GRCh37 |
| NC_000017.9:g.35116788G>T | NCBI36 |
| NG_007503.1:g.23870G>T , LRG_724:g.23870G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269571.10:c.93G>T MANE Select | ENSP00000269571.4:p.Met31Ile | |
| ENST00000269571.9:c.93G>T | ENSP00000269571.4:p.Met31Ile | |
| ENST00000406381.6:c.3G>T | ENSP00000385185.2:p.Met1Ile | |
| ENST00000445658.6:c.74-4919G>T | ENSP00000404047.2:n.74-4919G>T | |
| ENST00000541774.5:c.48G>T | ENSP00000446466.1:p.Met16Ile | |
| ENST00000578199.5:c.3G>T | ENSP00000462808.1:p.Met1Ile | |
| ENST00000578373.5:c.93G>T | ENSP00000463427.1:p.Met31Ile | |
| ENST00000578709.5:c.3G>T | ENSP00000463719.1:p.Met1Ile | |
| ENST00000582648.5:c.93G>T | ENSP00000462024.1:p.Met31Ile | |
| ENST00000582788.5:n.258G>T | ||
| ENST00000584099.1:c.3G>T | ENSP00000462270.1:p.Met1Ile | |
| ENST00000584450.5:c.93G>T | ENSP00000463714.1:p.Met31Ile | |
| ENST00000584601.5:c.3G>T | ENSP00000462438.1:p.Met1Ile | |
| ENST00000584908.5:n.105G>T | ||
| NM_001005862.2:c.3G>T , LRG_724t1:c.3G>T | NP_001005862.1:p.Met1Ile | |
| NM_001289936.1:c.48G>T , LRG_724t4:c.48G>T | NP_001276865.1:p.Met16Ile | |
| NM_001289937.1:c.93G>T | NP_001276866.1:p.Met31Ile | |
| NM_001289938.1:c.3G>T , LRG_724t3:c.3G>T | NP_001276867.1:p.Met1Ile | |
| NM_004448.3:c.93G>T , LRG_724t2:c.93G>T | NP_004439.2:p.Met31Ile | |
| NR_110535.1:n.354G>T | ||
| XM_024450641.1:c.93G>T | XP_024306409.1:p.Met31Ile | |
| XM_024450642.1:c.48G>T | XP_024306410.1:p.Met16Ile | |
| XM_024450643.1:c.3G>T | XP_024306411.1:p.Met1Ile | |
| NM_001005862.3:c.3G>T | NP_001005862.1:p.Met1Ile | |
| NM_001289936.2:c.48G>T | NP_001276865.1:p.Met16Ile | |
| NM_001289937.2:c.93G>T | NP_001276866.1:p.Met31Ile | |
| NM_001289938.2:c.3G>T | NP_001276867.1:p.Met1Ile | |
| NM_001382782.1:c.3G>T | NP_001369711.1:p.Met1Ile | |
| NM_001382783.1:c.3G>T | NP_001369712.1:p.Met1Ile | |
| NM_001382784.1:c.93G>T | NP_001369713.1:p.Met31Ile | |
| NM_001382785.1:c.93G>T | NP_001369714.1:p.Met31Ile | |
| NM_001382786.1:c.93G>T | NP_001369715.1:p.Met31Ile | |
| NM_001382787.1:c.93G>T | NP_001369716.1:p.Met31Ile | |
| NM_001382788.1:c.93G>T | NP_001369717.1:p.Met31Ile | |
| NM_001382789.1:c.93G>T | NP_001369718.1:p.Met31Ile | |
| NM_001382790.1:c.93G>T | NP_001369719.1:p.Met31Ile | |
| NM_001382791.1:c.93G>T | NP_001369720.1:p.Met31Ile | |
| NM_001382792.1:c.93G>T | NP_001369721.1:p.Met31Ile | |
| NM_001382793.1:c.93G>T | NP_001369722.1:p.Met31Ile | |
| NM_001382794.1:c.93G>T | NP_001369723.1:p.Met31Ile | |
| NM_001382795.1:c.93G>T | NP_001369724.1:p.Met31Ile | |
| NM_001382796.1:c.93G>T | NP_001369725.1:p.Met31Ile | |
| NM_001382797.1:c.93G>T | NP_001369726.1:p.Met31Ile | |
| NM_001382798.1:c.93G>T | NP_001369727.1:p.Met31Ile | |
| NM_001382799.1:c.93G>T | NP_001369728.1:p.Met31Ile | |
| NM_001382800.1:c.93G>T | NP_001369729.1:p.Met31Ile | |
| NM_001382801.1:c.93G>T | NP_001369730.1:p.Met31Ile | |
| NM_001382802.1:c.93G>T | NP_001369731.1:p.Met31Ile | |
| NM_001382803.1:c.93G>T | NP_001369732.1:p.Met31Ile | |
| NM_001382804.1:c.74-4919G>T | NP_001369733.1:n.74-4919G>T | |
| NM_001382805.1:c.93G>T | NP_001369734.1:p.Met31Ile | |
| NM_001382806.1:c.93G>T | NP_001369735.1:p.Met31Ile | |
| NM_004448.4:c.93G>T MANE Select | NP_004439.2:p.Met31Ile | |
| NR_110535.2:n.268G>T |