Linked Data
ClinVar Variation Id:
2879807
ClinVar RCV Id:
RCV003750406
dbSNP Id:
rs769507636
ExAC:
7:100231098 G / C
gnomAD v2:
7-100231098-G-C
gnomAD v4:
7-100633475-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100633475G>C , CM000669.2:g.100633475G>C | GRCh38 |
| NC_000007.13:g.100231098G>C , CM000669.1:g.100231098G>C | GRCh37 |
| NC_000007.12:g.100069034G>C | NCBI36 |
| NG_007989.1:g.13076C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000223051.8:c.555C>G MANE Select | ENSP00000223051.3:p.Arg185= | |
| ENST00000223051.7:c.555C>G | ENSP00000223051.3:p.Arg185= | |
| ENST00000431692.5:c.555C>G | ENSP00000413905.1:p.Arg185= | |
| ENST00000462107.1:c.555C>G | ENSP00000420525.1:p.Arg185= | |
| ENST00000465294.5:n.560C>G | ||
| ENST00000475011.1:n.84C>G | ||
| ENST00000476304.5:n.176C>G | ||
| NM_001206855.1:c.42C>G | NP_001193784.1:p.Arg14= | |
| NM_003227.3:c.555C>G | NP_003218.2:p.Arg185= | |
| XM_005250553.3:c.555C>G | XP_005250610.1:p.Arg185= | |
| XM_005250554.3:c.555C>G | XP_005250611.1:p.Arg185= | |
| NM_001206855.2:c.42C>G | NP_001193784.1:p.Arg14= | |
| XM_005250553.4:c.555C>G | XP_005250610.1:p.Arg185= | |
| XM_017012573.1:c.555C>G | XP_016868062.1:p.Arg185= | |
| NM_003227.4:c.555C>G MANE Select | NP_003218.2:p.Arg185= | |
| NM_001206855.3:c.42C>G | NP_001193784.1:p.Arg14= |