Linked Data
ClinVar Variation Id:
704379
dbSNP Id:
rs1007358932
gnomAD v2:
17-68171387-C-G
gnomAD v3:
17-70175246-C-G
gnomAD v4:
17-70175246-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70175246C>G , CM000679.2:g.70175246C>G | GRCh38 |
| NC_000017.10:g.68171387C>G , CM000679.1:g.68171387C>G | GRCh37 |
| NC_000017.9:g.65682982C>G | NCBI36 |
| NG_008798.1:g.10712C>G , LRG_328:g.10712C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000243457.4:c.207C>G MANE Select | ENSP00000243457.2:p.Leu69= | |
| ENST00000243457.3:c.207C>G | ENSP00000243457.2:p.Leu69= | |
| ENST00000535240.1:c.207C>G | ENSP00000441848.1:p.Leu69= | |
| NM_000891.2:c.207C>G , LRG_328t1:c.207C>G | NP_000882.1:p.Leu69= | |
| XM_011524779.1:c.207C>G | XP_011523081.1:p.Leu69= | |
| NM_000891.3:c.207C>G MANE Select | NP_000882.1:p.Leu69= |