Linked Data
ClinVar Variation Id:
1331036
ClinVar RCV Id:
RCV001812585
dbSNP Id:
rs33912272
gnomAD v2:
11-5248236-G-C
gnomAD v3:
11-5227006-G-C
gnomAD v4:
11-5227006-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5227006G>C , CM000673.2:g.5227006G>C | GRCh38 |
| NC_000011.9:g.5248236G>C , CM000673.1:g.5248236G>C | GRCh37 |
| NC_000011.8:g.5204812G>C | NCBI36 |
| NG_000007.3:g.70610C>G | |
| NG_059281.1:g.5066C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.16C>G | ENSP00000494175.1:p.Pro6Ala | |
| ENST00000335295.4:c.16C>G MANE Select | ENSP00000333994.3:p.Pro6Ala | |
| ENST00000380315.2:c.16C>G | ENSP00000369671.2:p.Pro6Ala | |
| ENST00000485743.1:n.67C>G | ||
| ENST00000633227.1:c.16C>G | ENSP00000488004.1:p.Pro6Ala | |
| NM_000518.4:c.16C>G | NP_000509.1:p.Pro6Ala | |
| NM_000518.5:c.16C>G MANE Select | NP_000509.1:p.Pro6Ala |