Linked Data
ClinVar Variation Id:
1556221
ClinVar RCV Id:
RCV002202201
dbSNP Id:
rs2101810642
MyVariant Identifiers:
chr1:g.172634925G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.172665785G>T , CM000663.2:g.172665785G>T | GRCh38 |
| NC_000001.10:g.172634925G>T , CM000663.1:g.172634925G>T | GRCh37 |
| NC_000001.9:g.170901548G>T | NCBI36 |
| NG_007269.1:g.11741G>T , LRG_58:g.11741G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367721.3:c.615G>T MANE Select | ENSP00000356694.2:p.Leu205= | |
| ENST00000340030.4:c.*185G>T | ENSP00000344739.3:n.*185G>T | |
| ENST00000367721.2:c.615G>T | ENSP00000356694.2:p.Leu205= | |
| NM_000639.2:c.615G>T | NP_000630.1:p.Leu205= | |
| NM_001302746.1:c.*185G>T | NP_001289675.1:n.*185G>T | |
| NM_000639.3:c.615G>T MANE Select | NP_000630.1:p.Leu205= | |
| NM_001302746.2:c.*185G>T | NP_001289675.1:n.*185G>T |