Linked Data
dbSNP Id:
rs917303898
gnomAD v4:
5-37052308-A-G
MyVariant Identifiers:
chr5:g.37052308A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37052308A>G , CM000667.2:g.37052308A>G | GRCh38 |
| NC_000005.9:g.37052410A>G , CM000667.1:g.37052410A>G | GRCh37 |
| NC_000005.8:g.37088167A>G | NCBI36 |
| NG_006987.1:g.180426A>G | |
| NG_006987.2:g.180426A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282516.13:c.7063-58A>G MANE Select | ENSP00000282516.8:n.7063-58A>G | |
| ENST00000652901.1:c.7063-58A>G | ENSP00000499536.1:n.7063-58A>G | |
| ENST00000282516.12:c.7063-58A>G | ENSP00000282516.8:n.7063-58A>G | |
| ENST00000448238.2:c.7063-58A>G | ENSP00000406266.2:n.7063-58A>G | |
| ENST00000514335.1:n.945-58A>G | ||
| ENST00000621733.1:c.1-12270A>G | ENSP00000480694.1:n.1-12270A>G | |
| NM_015384.4:c.7063-58A>G | NP_056199.2:n.7063-58A>G | |
| NM_133433.3:c.7063-58A>G | NP_597677.2:n.7063-58A>G | |
| XM_005248280.2:c.7063-58A>G | XP_005248337.1:n.7063-58A>G | |
| XM_005248282.3:c.6319-58A>G | XP_005248339.2:n.6319-58A>G | |
| XM_006714467.2:c.7063-58A>G | XP_006714530.1:n.7063-58A>G | |
| XM_006714468.1:c.6865-58A>G | XP_006714531.1:n.6865-58A>G | |
| XM_011514014.1:c.6682-58A>G | XP_011512316.1:n.6682-58A>G | |
| XM_011514015.1:c.7063-58A>G | XP_011512317.1:n.7063-58A>G | |
| XM_005248280.3:c.7063-58A>G | XP_005248337.1:n.7063-58A>G | |
| XM_005248282.5:c.6403-58A>G | XP_005248339.3:n.6403-58A>G | |
| XM_006714468.2:c.6865-58A>G | XP_006714531.1:n.6865-58A>G | |
| XM_017009329.1:c.7063-58A>G | XP_016864818.1:n.7063-58A>G | |
| XM_017009330.2:c.5446-58A>G | XP_016864819.1:n.5446-58A>G | |
| XM_017009331.1:c.5437-58A>G | XP_016864820.1:n.5437-58A>G | |
| NM_133433.4:c.7063-58A>G MANE Select | NP_597677.2:n.7063-58A>G | |
| NM_015384.5:c.7063-58A>G | NP_056199.2:n.7063-58A>G |