Linked Data
dbSNP Id:
rs549339139
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115731077C>T , CM000663.2:g.115731077C>T | GRCh38 |
| NC_000001.10:g.116273698C>T , CM000663.1:g.116273698C>T | GRCh37 |
| NC_000001.9:g.116075221C>T | NCBI36 |
| NG_008802.1:g.42729G>A , LRG_404:g.42729G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.425+1037G>A | ENSP00000518226.1:n.425+1037G>A | |
| ENST00000261448.6:c.606+1824G>A MANE Select | ENSP00000261448.5:n.606+1824G>A | |
| ENST00000261448.5:c.606+1824G>A | ENSP00000261448.5:n.606+1824G>A | |
| ENST00000488931.1:n.122+1037G>A | ||
| NM_001232.3:c.606+1824G>A , LRG_404t1:c.606+1824G>A | NP_001223.2:n.606+1824G>A | |
| NM_001232.4:c.606+1824G>A MANE Select | NP_001223.2:n.606+1824G>A |