Linked Data
dbSNP Id:
rs761622783
gnomAD v3:
2-240877567-G-C
gnomAD v4:
2-240877567-G-C
COSMIC:
COSM4561257
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877567G>C , CM000664.2:g.240877567G>C | GRCh38 |
| NC_000002.11:g.241816984G>C , CM000664.1:g.241816984G>C | GRCh37 |
| NC_000002.10:g.241465657G>C | NCBI36 |
| NG_008005.1:g.13823G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.877G>C MANE Select | ENSP00000302620.3:p.Glu293Gln | |
| ENST00000307503.3:c.877G>C | ENSP00000302620.3:p.Glu293Gln | |
| ENST00000470255.1:n.655G>C | ||
| NM_000030.2:c.877G>C | NP_000021.1:p.Glu293Gln | |
| NM_000030.3:c.877G>C MANE Select | NP_000021.1:p.Glu293Gln |