Linked Data
ClinVar Variation Id:
3229
dbSNP Id:
rs267606971
gnomAD v2:
14-77769283-G-A
gnomAD v4:
14-77302940-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.77302940G>A , CM000676.2:g.77302940G>A | GRCh38 |
| NC_000014.8:g.77769283G>A , CM000676.1:g.77769283G>A | GRCh37 |
| NC_000014.7:g.76839036G>A | NCBI36 |
| NG_008897.1:g.22943C>T , LRG_844:g.22943C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553863.6:c.110-1691C>T | ENSP00000508202.1:n.110-1691C>T | |
| ENST00000555675.6:n.1816C>T | ||
| ENST00000556394.2:c.357+1752C>T | ENSP00000451967.2:n.357+1752C>T | |
| ENST00000556880.6:n.575C>T | ||
| ENST00000682247.1:c.551C>T | ENSP00000507213.1:p.Thr184Met | |
| ENST00000682377.1:c.131C>T | ENSP00000507494.1:p.Thr44Met | |
| ENST00000682382.1:c.495+1752C>T | ||
| ENST00000682395.1:n.280C>T | ||
| ENST00000682459.1:n.215C>T | ||
| ENST00000682467.1:c.551C>T | ENSP00000508062.1:p.Thr184Met | |
| ENST00000682795.1:c.551C>T | ENSP00000507574.1:p.Thr184Met | |
| ENST00000682895.1:n.267C>T | ||
| ENST00000682955.1:n.211+1752C>T | ||
| ENST00000683188.1:c.342+1752C>T | ||
| ENST00000683300.1:c.109+1752C>T | ENSP00000507630.1:n.109+1752C>T | |
| ENST00000683328.1:c.109+1752C>T | ENSP00000508096.1:n.109+1752C>T | |
| ENST00000683380.1:n.215C>T | ||
| ENST00000683551.1:c.4C>T | ||
| ENST00000683828.1:c.420C>T | ||
| ENST00000684102.1:n.1833C>T | ||
| ENST00000684259.1:n.402C>T | ||
| ENST00000684549.1:n.367+1752C>T | ||
| ENST00000261534.9:c.551C>T MANE Select | ENSP00000261534.4:p.Thr184Met | |
| ENST00000261534.8:c.551C>T | ENSP00000261534.4:p.Thr184Met | |
| ENST00000452340.7:n.574C>T | ||
| ENST00000553863.5:n.215C>T | ||
| ENST00000554948.1:c.278C>T | ENSP00000452060.1:p.Thr93Met | |
| ENST00000555675.5:n.267C>T | ||
| ENST00000556326.5:c.*217C>T | ENSP00000450630.1:n.*217C>T | |
| ENST00000556880.5:n.575C>T | ||
| ENST00000557289.1:c.55+1752C>T | ENSP00000451115.1:n.55+1752C>T | |
| NM_013382.5:c.551C>T , LRG_844t1:c.551C>T | NP_037514.2:p.Thr184Met | |
| XM_011536675.1:c.551C>T | XP_011534977.1:p.Thr184Met | |
| XM_011536676.1:c.218C>T | XP_011534978.1:p.Thr73Met | |
| XM_011536677.1:c.547+1752C>T | XP_011534979.1:n.547+1752C>T | |
| XM_011536678.1:c.551C>T | XP_011534980.1:p.Thr184Met | |
| XM_011536679.1:c.-91+1752C>T | XP_011534981.1:n.-91+1752C>T | |
| XM_011536680.1:c.551C>T | XP_011534982.1:p.Thr184Met | |
| XR_943416.1:n.754C>T | ||
| XM_011536675.2:c.551C>T | XP_011534977.1:p.Thr184Met | |
| XM_011536676.2:c.218C>T | XP_011534978.1:p.Thr73Met | |
| XM_011536677.3:c.547+1752C>T | XP_011534979.1:n.547+1752C>T | |
| XR_001750279.1:n.751C>T | ||
| XR_001750282.1:n.755C>T | ||
| XR_943416.3:n.752C>T | ||
| NM_013382.6:c.551C>T | NP_037514.2:p.Thr184Met | |
| NM_013382.7:c.551C>T MANE Select | NP_037514.2:p.Thr184Met |