Linked Data
ClinVar Variation Id:
2923067
ClinVar RCV Id:
RCV003780185
dbSNP Id:
rs2101513936
MyVariant Identifiers:
chr1:g.17349196A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17022701A>G , CM000663.2:g.17022701A>G | GRCh38 |
| NC_000001.10:g.17349196A>G , CM000663.1:g.17349196A>G | GRCh37 |
| NC_000001.9:g.17221783A>G | NCBI36 |
| NG_012340.1:g.36470T>C , LRG_316:g.36470T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.501T>C | ENSP00000481376.2:p.Asp167= | |
| ENST00000491274.6:c.630T>C | ENSP00000480482.2:p.Asp210= | |
| ENST00000375499.8:c.672T>C MANE Select | ENSP00000364649.3:p.Asp224= | |
| ENST00000375499.7:c.672T>C | ENSP00000364649.3:p.Asp224= | |
| ENST00000475049.5:n.97T>C | ||
| ENST00000485092.5:n.336T>C | ||
| ENST00000485515.5:n.606T>C | ||
| NM_003000.2:c.672T>C , LRG_316t1:c.672T>C | NP_002991.2:p.Asp224= | |
| NM_003000.3:c.672T>C MANE Select | NP_002991.2:p.Asp224= |