Linked Data
ClinVar Variation Id:
1175217
ClinVar RCV Id:
RCV001530226
dbSNP Id:
rs2152010899
MyVariant Identifiers:
chr6:g.42689557C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721819C>A , CM000668.2:g.42721819C>A | GRCh38 |
| NC_000006.11:g.42689557C>A , CM000668.1:g.42689557C>A | GRCh37 |
| NC_000006.10:g.42797535C>A | NCBI36 |
| NG_009176.1:g.5802G>T | |
| NG_009176.2:g.5802G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.516G>T MANE Select | ENSP00000230381.5:p.Arg172= | |
| ENST00000230381.6:c.516G>T | ENSP00000230381.5:p.Arg172= | |
| NM_000322.4:c.516G>T | NP_000313.2:p.Arg172= | |
| XR_427834.2:n.1171G>T | ||
| XR_926295.1:n.1171G>T | ||
| XR_427834.4:n.1221G>T | ||
| XR_926295.3:n.1221G>T | ||
| NM_000322.5:c.516G>T MANE Select | NP_000313.2:p.Arg172= |