Linked Data
ClinVar Variation Id:
631
dbSNP Id:
rs74486803
ExAC:
12:103249093 C / A
gnomAD v2:
12-103249093-C-A
gnomAD v3:
12-102855315-C-A
gnomAD v4:
12-102855315-C-A
COSMIC:
COSM1188584
ERepo:
CA114371/MONDO:0009861/006
PubMed:
PMID:8088845
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102855315C>A , CM000674.2:g.102855315C>A | GRCh38 |
| NC_000012.11:g.103249093C>A , CM000674.1:g.103249093C>A | GRCh37 |
| NC_000012.10:g.101773223C>A | NCBI36 |
| NG_008690.1:g.67288G>T | |
| NG_008690.2:g.108096G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.527G>T MANE Select | ENSP00000448059.1:p.Arg176Leu | |
| ENST00000307000.7:c.512G>T | ENSP00000303500.2:p.Arg171Leu | |
| ENST00000549111.5:n.623G>T | ||
| ENST00000551988.5:n.548G>T | ||
| ENST00000553106.5:c.527G>T | ENSP00000448059.1:p.Arg176Leu | |
| NM_000277.1:c.527G>T | NP_000268.1:p.Arg176Leu | |
| XM_011538422.1:c.527G>T | XP_011536724.1:p.Arg176Leu | |
| NM_000277.2:c.527G>T | NP_000268.1:p.Arg176Leu | |
| NM_001354304.1:c.527G>T | NP_001341233.1:p.Arg176Leu | |
| XM_017019370.2:c.527G>T | XP_016874859.1:p.Arg176Leu | |
| NM_000277.3:c.527G>T MANE Select | NP_000268.1:p.Arg176Leu | |
| NM_001354304.2:c.527G>T | NP_001341233.1:p.Arg176Leu |