Linked Data
gnomAD v3:
6-29942334-A-G
gnomAD v4:
6-29942334-A-G
MyVariant Identifiers:
chr6:g.29910111A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29942334A>G , CM000668.2:g.29942334A>G | GRCh38 |
| NC_000006.11:g.29910111A>G , CM000668.1:g.29910111A>G | GRCh37 |
| NC_000006.10:g.30018090A>G | NCBI36 |
| NG_029217.2:g.4869A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706892.1:n.127-70A>G | ||
| ENST00000706893.1:c.-150-70A>G | ENSP00000516609.1:n.-150-70A>G | |
| ENST00000706894.1:c.-150-70A>G | ENSP00000516610.1:n.-150-70A>G | |
| ENST00000706895.1:n.127-70A>G | ||
| ENST00000706896.1:n.127-70A>G | ||
| ENST00000706897.1:n.127-70A>G | ||
| ENST00000706898.1:c.-150-70A>G | ENSP00000516611.1:n.-150-70A>G | |
| ENST00000706899.1:n.127-70A>G | ||
| ENST00000706901.1:c.-150-70A>G | ENSP00000516612.1:n.-150-70A>G | |
| ENST00000706902.1:c.-150-70A>G | ENSP00000516613.1:n.-150-70A>G | |
| ENST00000706903.1:c.-150-70A>G | ENSP00000516614.1:n.-150-70A>G | |
| ENST00000706904.1:c.-150-70A>G | ENSP00000516615.1:n.-150-70A>G | |
| ENST00000706905.1:c.-220A>G | ENSP00000516616.1:n.-220A>G | |
| ENST00000376806.9:c.-220A>G | ENSP00000366002.5:n.-220A>G | |
| ENST00000396634.5:c.-150-70A>G | ENSP00000379873.1:n.-150-70A>G | |
| ENST00000429656.1:n.734T>C |