Linked Data
ClinVar Variation Id:
305942
ClinVar RCV Id:
RCV000295595
dbSNP Id:
rs11233662
gnomAD v2:
11-71145970-T-C
gnomAD v3:
11-71434924-T-C
gnomAD v4:
11-71434924-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71434924T>C , CM000673.2:g.71434924T>C | GRCh38 |
| NC_000011.9:g.71145970T>C , CM000673.1:g.71145970T>C | GRCh37 |
| NC_000011.8:g.70823618T>C | NCBI36 |
| NG_012655.2:g.18508A>G , LRG_340:g.18508A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000525346.6:c.*451A>G | ENSP00000435707.3:n.*451A>G | |
| ENST00000526780.6:c.*451A>G | ENSP00000435668.2:n.*451A>G | |
| ENST00000682708.1:c.*451A>G | ENSP00000506866.1:n.*451A>G | |
| ENST00000683287.1:c.*451A>G | ENSP00000507607.1:n.*451A>G | |
| ENST00000683714.1:c.*642A>G | ENSP00000508207.1:n.*642A>G | |
| ENST00000684396.1:n.1919A>G | ||
| ENST00000685320.1:c.*451A>G | ENSP00000509319.1:n.*451A>G | |
| ENST00000690257.1:c.*451A>G | ENSP00000510750.1:n.*451A>G | |
| ENST00000355527.8:c.*451A>G MANE Select | ENSP00000347717.4:n.*451A>G | |
| ENST00000355527.7:c.*451A>G | ENSP00000347717.3:n.*451A>G | |
| ENST00000407721.6:c.*451A>G | ENSP00000384739.2:n.*451A>G | |
| ENST00000534795.5:c.319+2888A>G | ||
| NM_001163817.1:c.*451A>G | NP_001157289.1:n.*451A>G | |
| NM_001360.2:c.*451A>G , LRG_340t1:c.*451A>G | NP_001351.2:n.*451A>G | |
| XM_011544777.1:c.*642A>G | XP_011543079.1:n.*642A>G | |
| XM_011544777.2:c.*642A>G | XP_011543079.1:n.*642A>G | |
| NM_001163817.2:c.*451A>G | NP_001157289.1:n.*451A>G | |
| NM_001360.3:c.*451A>G MANE Select | NP_001351.2:n.*451A>G |