Linked Data
ClinVar Variation Id:
305949
dbSNP Id:
rs151230950
gnomAD v2:
11-71146302-C-T
gnomAD v3:
11-71435256-C-T
gnomAD v4:
11-71435256-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435256C>T , CM000673.2:g.71435256C>T | GRCh38 |
| NC_000011.9:g.71146302C>T , CM000673.1:g.71146302C>T | GRCh37 |
| NC_000011.8:g.70823950C>T | NCBI36 |
| NG_012655.2:g.18176G>A , LRG_340:g.18176G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.*119G>A | ENSP00000435707.3:n.*119G>A | |
| ENST00000526780.6:c.*119G>A | ENSP00000435668.2:n.*119G>A | |
| ENST00000682708.1:c.*119G>A | ENSP00000506866.1:n.*119G>A | |
| ENST00000683287.1:c.*119G>A | ENSP00000507607.1:n.*119G>A | |
| ENST00000683714.1:c.*310G>A | ENSP00000508207.1:n.*310G>A | |
| ENST00000684396.1:n.1587G>A | ||
| ENST00000685320.1:c.*119G>A | ENSP00000509319.1:n.*119G>A | |
| ENST00000690257.1:c.*119G>A | ENSP00000510750.1:n.*119G>A | |
| ENST00000355527.8:c.*119G>A MANE Select | ENSP00000347717.4:n.*119G>A | |
| ENST00000355527.7:c.*119G>A | ENSP00000347717.3:n.*119G>A | |
| ENST00000407721.6:c.*119G>A | ENSP00000384739.2:n.*119G>A | |
| ENST00000533800.5:c.612-66G>A | ENSP00000435011.1:n.612-66G>A | |
| ENST00000534795.5:c.319+2556G>A | ||
| NM_001163817.1:c.*119G>A | NP_001157289.1:n.*119G>A | |
| NM_001360.2:c.*119G>A , LRG_340t1:c.*119G>A | NP_001351.2:n.*119G>A | |
| XM_011544777.1:c.*310G>A | XP_011543079.1:n.*310G>A | |
| XM_011544777.2:c.*310G>A | XP_011543079.1:n.*310G>A | |
| NM_001163817.2:c.*119G>A | NP_001157289.1:n.*119G>A | |
| NM_001360.3:c.*119G>A MANE Select | NP_001351.2:n.*119G>A |