Linked Data
ClinVar Variation Id:
1557836
ClinVar RCV Id:
RCV002197370
dbSNP Id:
rs1590143219
gnomAD v4:
8-19954184-T-C
MyVariant Identifiers:
chr8:g.19811695T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19954184T>C , CM000670.2:g.19954184T>C | GRCh38 |
| NC_000008.10:g.19811695T>C , CM000670.1:g.19811695T>C | GRCh37 |
| NC_000008.9:g.19855975T>C | NCBI36 |
| NG_008855.1:g.20114T>C | |
| NG_008855.2:g.57468T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650287.1:c.606T>C MANE Select | ENSP00000497642.1:p.Asp202= | |
| ENST00000311322.8:c.606T>C | ENSP00000309757.6:p.Asp202= | |
| NM_000237.2:c.606T>C | NP_000228.1:p.Asp202= | |
| NM_000237.3:c.606T>C MANE Select | NP_000228.1:p.Asp202= |