Linked Data
ClinVar Variation Id:
331824
dbSNP Id:
rs151227843
ExAC:
2:166756333 G / A
gnomAD v2:
2-166756333-G-A
gnomAD v3:
2-165899823-G-A
gnomAD v4:
2-165899823-G-A
COSMIC:
COSM1400741
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.165899823G>A , CM000664.2:g.165899823G>A | GRCh38 |
| NC_000002.11:g.166756333G>A , CM000664.1:g.166756333G>A | GRCh37 |
| NC_000002.10:g.166464579G>A | NCBI36 |
| NG_030345.1:g.59016C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243344.8:c.2815C>T MANE Select | ENSP00000243344.7:p.Arg939Trp | |
| ENST00000652557.1:c.2815C>T | ENSP00000498617.1:p.Arg939Trp | |
| ENST00000679356.1:c.2815C>T | ENSP00000506245.1:p.Arg939Trp | |
| ENST00000679676.1:c.2704C>T | ENSP00000505492.1:p.Arg902Trp | |
| ENST00000679799.1:c.2815C>T | ENSP00000505208.1:p.Arg939Trp | |
| ENST00000679840.1:c.2815C>T | ENSP00000505248.1:p.Arg939Trp | |
| ENST00000679931.1:c.*1857C>T | ENSP00000505632.1:n.*1857C>T | |
| ENST00000679967.1:c.2815C>T | ENSP00000506607.1:p.Arg939Trp | |
| ENST00000680327.1:c.*1857C>T | ENSP00000506639.1:n.*1857C>T | |
| ENST00000680448.1:c.2815C>T | ENSP00000505921.1:p.Arg939Trp | |
| ENST00000680657.1:n.2926C>T | ||
| ENST00000680690.1:c.*2067C>T | ENSP00000506121.1:n.*2067C>T | |
| ENST00000680888.1:c.2815C>T | ENSP00000506276.1:p.Arg939Trp | |
| ENST00000680925.1:n.845C>T | ||
| ENST00000680947.1:c.*2087C>T | ENSP00000506496.1:n.*2087C>T | |
| ENST00000681024.1:c.2815C>T | ENSP00000506449.1:p.Arg939Trp | |
| ENST00000681083.1:c.*2549C>T | ENSP00000506095.1:n.*2549C>T | |
| ENST00000681167.1:n.2689C>T | ||
| ENST00000681483.1:c.2815C>T | ENSP00000505499.1:p.Arg939Trp | |
| ENST00000681502.1:c.*2239C>T | ENSP00000505644.1:n.*2239C>T | |
| ENST00000681606.1:c.2815C>T | ENSP00000505354.1:p.Arg939Trp | |
| ENST00000681819.1:c.2815C>T | ENSP00000505673.1:p.Arg939Trp | |
| ENST00000681952.1:c.2815C>T | ENSP00000506400.1:p.Arg939Trp | |
| ENST00000243344.7:c.2815C>T | ENSP00000243344.7:p.Arg939Trp | |
| ENST00000484129.1:n.290C>T | ||
| NM_024753.4:c.2815C>T | NP_079029.3:p.Arg939Trp | |
| XM_006712761.1:c.2815C>T | XP_006712824.1:p.Arg939Trp | |
| XM_011511870.1:c.2248C>T | XP_011510172.1:p.Arg750Trp | |
| XM_011511871.1:c.2065C>T | XP_011510173.1:p.Arg689Trp | |
| XM_011511872.1:c.*17C>T | XP_011510174.1:n.*17C>T | |
| XM_011511871.3:c.2065C>T | XP_011510173.1:p.Arg689Trp | |
| XM_011511872.2:c.*17C>T | XP_011510174.1:n.*17C>T | |
| XM_017004967.1:c.2815C>T | XP_016860456.1:p.Arg939Trp | |
| XM_017004968.2:c.2161C>T | XP_016860457.1:p.Arg721Trp | |
| XM_017004969.1:c.1816C>T | XP_016860458.1:p.Arg606Trp | |
| NM_024753.5:c.2815C>T MANE Select | NP_079029.3:p.Arg939Trp |