Linked Data
dbSNP Id:
rs1037317996
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160882300C>G , CM000663.2:g.160882300C>G | GRCh38 |
| NC_000001.10:g.160852090C>G , CM000663.1:g.160852090C>G | GRCh37 |
| NC_000001.9:g.159118714C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000326245.4:c.158-96G>C MANE Select | ENSP00000323587.3:n.158-96G>C | |
| ENST00000326245.3:c.158-96G>C | ENSP00000323587.3:n.158-96G>C | |
| NM_017625.2:c.158-96G>C | NP_060095.2:n.158-96G>C | |
| NM_017625.3:c.158-96G>C MANE Select | NP_060095.2:n.158-96G>C |