Linked Data
dbSNP Id:
rs80356836
gnomAD v4:
17-43094535-C-T
MyVariant Identifiers:
chr17:g.41246552C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43094535C>T , CM000679.2:g.43094535C>T | GRCh38 |
| NC_000017.10:g.41246552C>T , CM000679.1:g.41246552C>T | GRCh37 |
| NC_000017.9:g.38500078C>T | NCBI36 |
| NG_005905.2:g.123449G>A , LRG_292:g.123449G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000354071.8:n.1060G>A | ||
| ENST00000461574.2:c.996G>A | ENSP00000417241.2:p.Arg332= | |
| ENST00000470026.6:c.996G>A | ENSP00000419274.2:p.Arg332= | |
| ENST00000473961.6:c.870G>A | ENSP00000420201.2:p.Arg290= | |
| ENST00000476777.6:c.993G>A | ENSP00000417554.2:p.Arg331= | |
| ENST00000477152.6:c.918G>A | ENSP00000419988.2:p.Arg306= | |
| ENST00000478531.6:c.784+209G>A | ENSP00000420412.2:n.784+209G>A | |
| ENST00000489037.2:c.918G>A | ENSP00000420781.2:p.Arg306= | |
| ENST00000493919.6:c.646+209G>A | ENSP00000418819.2:n.646+209G>A | |
| ENST00000494123.6:c.996G>A | ENSP00000419103.2:p.Arg332= | |
| ENST00000497488.2:c.108G>A | ENSP00000418986.2:p.Arg36= | |
| ENST00000618469.2:c.996G>A | ENSP00000478114.2:p.Arg332= | |
| ENST00000634433.2:c.873G>A | ENSP00000489431.2:p.Arg291= | |
| ENST00000644379.2:c.996G>A | ENSP00000496570.2:p.Arg332= | |
| ENST00000644555.2:c.646+209G>A | ENSP00000494614.2:n.646+209G>A | |
| ENST00000652672.2:c.855G>A | ENSP00000498906.2:p.Arg285= | |
| ENST00000484087.6:c.664+209G>A | ENSP00000419481.2:n.664+209G>A | |
| ENST00000700182.1:c.706+209G>A | ENSP00000514849.1:n.706+209G>A | |
| ENST00000700183.1:c.*1004G>A | ENSP00000514850.1:n.*1004G>A | |
| ENST00000357654.9:c.996G>A MANE Select | ENSP00000350283.3:p.Arg332= | |
| ENST00000471181.7:c.996G>A | ENSP00000418960.2:p.Arg332= | |
| ENST00000642945.1:c.*870G>A | ENSP00000495897.1:n.*870G>A | |
| ENST00000652672.1:c.855G>A | ENSP00000498906.1:p.Arg285= | |
| ENST00000352993.7:c.670+1311G>A | ENSP00000312236.5:n.670+1311G>A | |
| ENST00000354071.7:c.996G>A | ENSP00000326002.7:p.Arg332= | |
| ENST00000357654.7:c.996G>A | ENSP00000350283.3:p.Arg332= | |
| ENST00000412061.3:c.347G>A | ||
| ENST00000461221.5:c.*779G>A | ENSP00000418548.1:n.*779G>A | |
| ENST00000468300.5:c.787+209G>A | ENSP00000417148.1:n.787+209G>A | |
| ENST00000470026.5:c.996G>A | ENSP00000419274.1:p.Arg332= | |
| ENST00000471181.6:c.996G>A | ENSP00000418960.2:p.Arg332= | |
| ENST00000473961.5:c.593G>A | ||
| ENST00000477152.5:c.918G>A | ENSP00000419988.1:p.Arg306= | |
| ENST00000478531.5:c.784+209G>A | ENSP00000420412.1:n.784+209G>A | |
| ENST00000484087.5:c.409+209G>A | ENSP00000419481.1:n.409+209G>A | |
| ENST00000487825.5:c.412+209G>A | ENSP00000418212.1:n.412+209G>A | |
| ENST00000491747.6:c.787+209G>A | ENSP00000420705.2:n.787+209G>A | |
| ENST00000492859.5:c.*932G>A | ENSP00000420253.1:n.*932G>A | |
| ENST00000493795.5:c.855G>A | ENSP00000418775.1:p.Arg285= | |
| ENST00000493919.5:c.646+209G>A | ENSP00000418819.1:n.646+209G>A | |
| ENST00000494123.5:c.996G>A | ENSP00000419103.1:p.Arg332= | |
| ENST00000497488.1:c.108G>A | ENSP00000418986.1:p.Arg36= | |
| ENST00000586385.5:c.5-30584G>A | ENSP00000465818.1:n.5-30584G>A | |
| ENST00000591534.5:c.-43-20014G>A | ENSP00000467329.1:n.-43-20014G>A | |
| ENST00000591849.5:c.-99+30736G>A | ENSP00000465347.1:n.-99+30736G>A | |
| ENST00000634433.1:c.873G>A | ENSP00000489431.1:p.Arg291= | |
| NM_007294.3:c.996G>A , LRG_292t1:c.996G>A | NP_009225.1:p.Arg332= | |
| NM_007297.3:c.855G>A | NP_009228.2:p.Arg285= | |
| NM_007298.3:c.787+209G>A | NP_009229.2:n.787+209G>A | |
| NM_007299.3:c.787+209G>A | NP_009230.2:n.787+209G>A | |
| NM_007300.3:c.996G>A | NP_009231.2:p.Arg332= | |
| NR_027676.1:n.1132G>A | ||
| NM_007294.4:c.996G>A MANE Select | NP_009225.1:p.Arg332= | |
| NM_007297.4:c.855G>A | NP_009228.2:p.Arg285= | |
| NM_007299.4:c.787+209G>A | NP_009230.2:n.787+209G>A | |
| NM_007300.4:c.996G>A | NP_009231.2:p.Arg332= | |
| NR_027676.2:n.1173G>A |