Linked Data
dbSNP Id:
rs1270608441
gnomAD v2:
17-39768878-T-C
gnomAD v3:
17-41612626-T-C
gnomAD v4:
17-41612626-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612626T>C , CM000679.2:g.41612626T>C | GRCh38 |
| NC_000017.10:g.39768878T>C , CM000679.1:g.39768878T>C | GRCh37 |
| NC_000017.9:g.37022404T>C | NCBI36 |
| NG_008301.1:g.5202A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.63A>G MANE Select | ENSP00000301653.3:p.Gly21= | |
| ENST00000301653.8:c.63A>G | ENSP00000301653.3:p.Gly21= | |
| ENST00000588319.1:n.140A>G | ||
| ENST00000590990.1:c.63A>G | ENSP00000467105.1:p.Gly21= | |
| ENST00000593067.1:c.-313+164A>G | ENSP00000467124.1:n.-313+164A>G | |
| NM_005557.3:c.63A>G | NP_005548.2:p.Gly21= | |
| NM_005557.4:c.63A>G MANE Select | NP_005548.2:p.Gly21= |