Linked Data
dbSNP Id:
rs11539506
gnomAD v4:
19-4099274-G-C
MyVariant Identifiers:
chr19:g.4099272G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4099274G>C , CM000681.2:g.4099274G>C | GRCh38 |
| NC_000019.9:g.4099272G>C , CM000681.1:g.4099272G>C | GRCh37 |
| NC_000019.8:g.4050272G>C | NCBI36 |
| NG_007996.1:g.29855C>G , LRG_750:g.29855C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394867.9:n.1285C>G | ||
| ENST00000687128.1:n.1285C>G | ||
| ENST00000688002.1:n.1140C>G | ||
| ENST00000689792.1:n.750C>G | ||
| ENST00000262948.10:c.846C>G MANE Select | ENSP00000262948.4:p.Pro282= | |
| ENST00000262948.9:c.846C>G | ENSP00000262948.3:p.Pro282= | |
| ENST00000394867.8:c.555C>G | ENSP00000378336.1:p.Pro185= | |
| ENST00000593364.5:n.793C>G | ||
| ENST00000595715.1:n.661C>G | ||
| ENST00000597263.5:n.169+1745C>G | ||
| ENST00000599021.1:c.29+1745C>G | ||
| ENST00000600584.5:n.1406C>G | ||
| ENST00000601786.5:n.1147C>G | ||
| NM_030662.3:c.846C>G , LRG_750t1:c.846C>G | NP_109587.1:p.Pro282= | |
| XM_006722799.2:c.705+1745C>G | XP_006722862.1:n.705+1745C>G | |
| XM_011528133.1:c.276C>G | XP_011526435.1:p.Pro92= | |
| XM_017026989.1:c.846C>G | XP_016882478.1:p.Pro282= | |
| XM_017026990.1:c.705+1745C>G | XP_016882479.1:n.705+1745C>G | |
| NM_030662.4:c.846C>G MANE Select | NP_109587.1:p.Pro282= |