Linked Data
ClinVar Variation Id:
1307214
ClinVar RCV Id:
RCV001760632
dbSNP Id:
rs200427972
gnomAD v2:
11-44148405-G-C
gnomAD v3:
11-44126855-G-C
gnomAD v4:
11-44126855-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.44126855G>C , CM000673.2:g.44126855G>C | GRCh38 |
| NC_000011.9:g.44148405G>C , CM000673.1:g.44148405G>C | GRCh37 |
| NC_000011.8:g.44104981G>C | NCBI36 |
| NG_007560.1:g.36307G>C , LRG_494:g.36307G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343631.4:c.979G>C | ENSP00000342656.3:p.Gly327Arg | |
| ENST00000395673.8:c.979G>C | ENSP00000379032.4:p.Gly327Arg | |
| ENST00000531161.6:n.1138G>C | ||
| ENST00000682359.1:c.939+1871G>C | ENSP00000508226.1:n.939+1871G>C | |
| ENST00000682711.1:c.-544+31003G>C | ENSP00000506803.1:n.-544+31003G>C | |
| ENST00000682815.1:c.979G>C | ENSP00000507234.1:p.Gly327Arg | |
| ENST00000682947.1:n.1153G>C | ||
| ENST00000682993.1:c.979G>C | ENSP00000507580.1:p.Gly327Arg | |
| ENST00000683000.1:c.979G>C | ENSP00000508361.1:p.Gly327Arg | |
| ENST00000683299.1:n.1396G>C | ||
| ENST00000683870.1:c.979G>C | ENSP00000507922.1:p.Gly327Arg | |
| ENST00000683881.1:n.3540G>C | ||
| ENST00000684039.1:c.979G>C | ENSP00000507677.1:p.Gly327Arg | |
| ENST00000684124.1:c.979G>C | ENSP00000508332.1:p.Gly327Arg | |
| ENST00000684533.1:c.744-3190G>C | ENSP00000507915.1:n.744-3190G>C | |
| ENST00000533608.7:c.979G>C MANE Select | ENSP00000431173.2:p.Gly327Arg | |
| ENST00000343631.3:c.979G>C | ENSP00000342656.3:p.Gly327Arg | |
| ENST00000358681.8:c.979G>C | ENSP00000351509.4:p.Gly327Arg | |
| ENST00000395673.7:c.1078G>C | ENSP00000379032.3:p.Gly360Arg | |
| ENST00000531161.5:n.156G>C | ||
| ENST00000533608.5:c.979G>C | ENSP00000431173.1:p.Gly327Arg | |
| NM_000401.3:c.1078G>C , LRG_494t1:c.1078G>C | NP_000392.3:p.Gly360Arg | |
| NM_001178083.1:c.979G>C | NP_001171554.1:p.Gly327Arg | |
| NM_207122.1:c.979G>C , LRG_494t2:c.979G>C | NP_997005.1:p.Gly327Arg | |
| XM_011519950.1:c.1117G>C | XP_011518252.1:p.Gly373Arg | |
| XM_011519951.1:c.1018G>C | XP_011518253.1:p.Gly340Arg | |
| XM_024448383.1:c.1117G>C | XP_024304151.1:p.Gly373Arg | |
| NM_001178083.2:c.979G>C | NP_001171554.1:p.Gly327Arg | |
| NM_207122.2:c.979G>C MANE Select | NP_997005.1:p.Gly327Arg | |
| NM_001178083.3:c.979G>C | NP_001171554.1:p.Gly327Arg | |
| NM_001389628.1:c.979G>C | NP_001376557.1:p.Gly327Arg | |
| NM_001389630.1:c.979G>C | NP_001376559.1:p.Gly327Arg |