Linked Data
dbSNP Id:
rs2101738756
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114709628G>A , CM000663.2:g.114709628G>A | GRCh38 |
| NC_000001.10:g.115252249G>A , CM000663.1:g.115252249G>A | GRCh37 |
| NC_000001.9:g.115053772G>A | NCBI36 |
| NG_007572.1:g.12267C>T , LRG_92:g.12267C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.391C>T MANE Select | ENSP00000358548.4:p.His131Tyr | |
| ENST00000369535.4:c.391C>T | ENSP00000358548.4:p.His131Tyr | |
| NM_002524.4:c.391C>T | NP_002515.1:p.His131Tyr | |
| NM_002524.5:c.391C>T MANE Select | NP_002515.1:p.His131Tyr |