Linked Data
dbSNP Id:
rs1802586022
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38146944A>G , CM000670.2:g.38146944A>G | GRCh38 |
| NC_000008.10:g.38004462A>G , CM000670.1:g.38004462A>G | GRCh37 |
| NC_000008.9:g.38123619A>G | NCBI36 |
| NG_011827.1:g.9139T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000276449.9:c.307-497T>C MANE Select | ENSP00000276449.3:n.307-497T>C | |
| ENST00000276449.8:c.307-497T>C | ENSP00000276449.3:n.307-497T>C | |
| ENST00000520114.1:n.794-497T>C | ||
| ENST00000521236.1:c.61-497T>C | ENSP00000430030.1:n.61-497T>C | |
| ENST00000522050.1:c.243-497T>C | ||
| NM_000349.2:c.307-497T>C | NP_000340.2:n.307-497T>C | |
| XM_006716392.1:c.307-497T>C | XP_006716455.1:n.307-497T>C | |
| NM_000349.3:c.307-497T>C MANE Select | NP_000340.2:n.307-497T>C |