Linked Data
dbSNP Id:
rs747001866
gnomAD v2:
17-39768428-G-C
gnomAD v3:
17-41612176-G-C
gnomAD v4:
17-41612176-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612176G>C , CM000679.2:g.41612176G>C | GRCh38 |
| NC_000017.10:g.39768428G>C , CM000679.1:g.39768428G>C | GRCh37 |
| NC_000017.9:g.37021954G>C | NCBI36 |
| NG_008301.1:g.5652C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.513C>G MANE Select | ENSP00000301653.3:p.Ile171Met | |
| ENST00000301653.8:c.513C>G | ENSP00000301653.3:p.Ile171Met | |
| ENST00000588319.1:n.590C>G | ||
| ENST00000593067.1:c.-202C>G | ENSP00000467124.1:n.-202C>G | |
| NM_005557.3:c.513C>G | NP_005548.2:p.Ile171Met | |
| NM_005557.4:c.513C>G MANE Select | NP_005548.2:p.Ile171Met |