Linked Data
ClinVar Variation Id:
838910
ClinVar RCV Id:
RCV001040561
dbSNP Id:
rs758389160
gnomAD v4:
7-128841181-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128841181G>C , CM000669.2:g.128841181G>C | GRCh38 |
| NC_000007.13:g.128481235G>C , CM000669.1:g.128481235G>C | GRCh37 |
| NC_000007.12:g.128268471G>C | NCBI36 |
| NG_011807.1:g.15753G>C , LRG_870:g.15753G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000325888.13:c.1825G>C MANE Select | ENSP00000327145.8:p.Glu609Gln | |
| ENST00000325888.12:c.1825G>C | ENSP00000327145.8:p.Glu609Gln | |
| ENST00000346177.6:c.1825G>C | ENSP00000344002.6:p.Glu609Gln | |
| NM_001127487.1:c.1825G>C | NP_001120959.1:p.Glu609Gln | |
| NM_001458.4:c.1825G>C , LRG_870t1:c.1825G>C | NP_001449.3:p.Glu609Gln | |
| NM_001127487.2:c.1825G>C | NP_001120959.1:p.Glu609Gln | |
| NM_001458.5:c.1825G>C MANE Select | NP_001449.3:p.Glu609Gln |