Linked Data
dbSNP Id:
rs749853877
ExAC:
17:61555337 C / G
gnomAD v2:
17-61555337-C-G
gnomAD v3:
17-63477976-C-G
gnomAD v4:
17-63477976-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63477976C>G , CM000679.2:g.63477976C>G | GRCh38 |
| NC_000017.10:g.61555337C>G , CM000679.1:g.61555337C>G | GRCh37 |
| NC_000017.9:g.58909069C>G | NCBI36 |
| NG_011648.1:g.5904C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290866.10:c.295C>G MANE Select | ENSP00000290866.4:p.Gln99Glu | |
| ENST00000290866.9:c.295C>G | ENSP00000290866.4:p.Gln99Glu | |
| ENST00000428043.5:c.295C>G | ENSP00000397593.2:p.Gln99Glu | |
| ENST00000579462.1:n.320C>G | ||
| ENST00000580318.1:n.484C>G | ||
| ENST00000582627.1:c.295C>G | ENSP00000462280.1:p.Gln99Glu | |
| ENST00000582678.5:c.295C>G | ENSP00000462995.1:p.Gln99Glu | |
| ENST00000583336.5:n.329C>G | ||
| ENST00000584529.5:n.329C>G | ||
| NM_000789.3:c.295C>G | NP_000780.1:p.Gln99Glu | |
| XM_005257110.1:c.-161C>G | XP_005257167.1:n.-161C>G | |
| NM_000789.4:c.295C>G MANE Select | NP_000780.1:p.Gln99Glu | |
| NM_001382700.1:c.60C>G | NP_001369629.1:p.Ala20= | |
| NM_001382701.1:c.-320C>G | NP_001369630.1:n.-320C>G |