Linked Data
ClinVar Variation Id:
2920471
ClinVar RCV Id:
RCV003654923
dbSNP Id:
rs142739534
MyVariant Identifiers:
chr1:g.115256486G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114713865G>C , CM000663.2:g.114713865G>C | GRCh38 |
| NC_000001.10:g.115256486G>C , CM000663.1:g.115256486G>C | GRCh37 |
| NC_000001.9:g.115058009G>C | NCBI36 |
| NG_007572.1:g.8030C>G , LRG_92:g.8030C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.225C>G MANE Select | ENSP00000358548.4:p.Gly75= | |
| ENST00000369535.4:c.225C>G | ENSP00000358548.4:p.Gly75= | |
| NM_002524.4:c.225C>G | NP_002515.1:p.Gly75= | |
| NM_002524.5:c.225C>G MANE Select | NP_002515.1:p.Gly75= |