Linked Data
ClinVar Variation Id:
261785
dbSNP Id:
rs148866170
ExAC:
2:166786809 G / C
gnomAD v2:
2-166786809-G-C
gnomAD v3:
2-165930299-G-C
gnomAD v4:
2-165930299-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.165930299G>C , CM000664.2:g.165930299G>C | GRCh38 |
| NC_000002.11:g.166786809G>C , CM000664.1:g.166786809G>C | GRCh37 |
| NC_000002.10:g.166495055G>C | NCBI36 |
| NG_030345.1:g.28540C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243344.8:c.960C>G MANE Select | ENSP00000243344.7:p.Asn320Lys | |
| ENST00000652557.1:c.960C>G | ENSP00000498617.1:p.Asn320Lys | |
| ENST00000679356.1:c.960C>G | ENSP00000506245.1:p.Asn320Lys | |
| ENST00000679671.1:n.1073C>G | ||
| ENST00000679676.1:c.849C>G | ENSP00000505492.1:p.Asn283Lys | |
| ENST00000679799.1:c.960C>G | ENSP00000505208.1:p.Asn320Lys | |
| ENST00000679840.1:c.960C>G | ENSP00000505248.1:p.Asn320Lys | |
| ENST00000679931.1:c.*2C>G | ENSP00000505632.1:n.*2C>G | |
| ENST00000679967.1:c.960C>G | ENSP00000506607.1:p.Asn320Lys | |
| ENST00000680225.1:n.219C>G | ||
| ENST00000680327.1:c.*2C>G | ENSP00000506639.1:n.*2C>G | |
| ENST00000680448.1:c.960C>G | ENSP00000505921.1:p.Asn320Lys | |
| ENST00000680657.1:n.1071C>G | ||
| ENST00000680690.1:c.*212C>G | ENSP00000506121.1:n.*212C>G | |
| ENST00000680888.1:c.960C>G | ENSP00000506276.1:p.Asn320Lys | |
| ENST00000680947.1:c.*232C>G | ENSP00000506496.1:n.*232C>G | |
| ENST00000681024.1:c.960C>G | ENSP00000506449.1:p.Asn320Lys | |
| ENST00000681083.1:c.*694C>G | ENSP00000506095.1:n.*694C>G | |
| ENST00000681167.1:n.834C>G | ||
| ENST00000681483.1:c.960C>G | ENSP00000505499.1:p.Asn320Lys | |
| ENST00000681502.1:c.*384C>G | ENSP00000505644.1:n.*384C>G | |
| ENST00000681606.1:c.960C>G | ENSP00000505354.1:p.Asn320Lys | |
| ENST00000681819.1:c.960C>G | ENSP00000505673.1:p.Asn320Lys | |
| ENST00000681952.1:c.960C>G | ENSP00000506400.1:p.Asn320Lys | |
| ENST00000243344.7:c.960C>G | ENSP00000243344.7:p.Asn320Lys | |
| ENST00000464374.5:n.1000C>G | ||
| NM_024753.4:c.960C>G | NP_079029.3:p.Asn320Lys | |
| XM_006712761.1:c.960C>G | XP_006712824.1:p.Asn320Lys | |
| XM_011511870.1:c.393C>G | XP_011510172.1:p.Asn131Lys | |
| XM_011511871.1:c.210C>G | XP_011510173.1:p.Asn70Lys | |
| XM_011511872.1:c.960C>G | XP_011510174.1:p.Asn320Lys | |
| XM_011511871.3:c.210C>G | XP_011510173.1:p.Asn70Lys | |
| XM_011511872.2:c.960C>G | XP_011510174.1:p.Asn320Lys | |
| XM_017004967.1:c.960C>G | XP_016860456.1:p.Asn320Lys | |
| XM_017004968.2:c.306C>G | XP_016860457.1:p.Asn102Lys | |
| XM_017004969.1:c.-40C>G | XP_016860458.1:n.-40C>G | |
| NM_024753.5:c.960C>G MANE Select | NP_079029.3:p.Asn320Lys |