Linked Data
dbSNP Id:
rs1561121754
gnomAD v2:
5-54529089-T-C
gnomAD v3:
5-55233261-T-C
gnomAD v4:
5-55233261-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55233261T>C , CM000667.2:g.55233261T>C | GRCh38 |
| NC_000005.9:g.54529089T>C , CM000667.1:g.54529089T>C | GRCh37 |
| NC_000005.8:g.54564846T>C | NCBI36 |
| NG_034201.1:g.5457A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.263A>G MANE Select | ENSP00000282572.4:p.Gln88Arg | |
| ENST00000282572.4:c.263A>G | ENSP00000282572.4:p.Gln88Arg | |
| ENST00000501463.2:c.263A>G | ENSP00000422485.1:p.Gln88Arg | |
| NM_021147.4:c.263A>G | NP_066970.3:p.Gln88Arg | |
| NR_125346.1:n.457A>G | ||
| NR_125347.1:n.457A>G | ||
| NM_021147.5:c.263A>G MANE Select | NP_066970.3:p.Gln88Arg | |
| NR_125346.2:n.348A>G | ||
| NR_125347.2:n.348A>G |