Linked Data
dbSNP Id:
rs1050137722
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48504999T>C , CM000677.2:g.48504999T>C | GRCh38 |
| NC_000015.9:g.48797196T>C , CM000677.1:g.48797196T>C | GRCh37 |
| NC_000015.8:g.46584488T>C | NCBI36 |
| NG_008805.2:g.145790A>G , LRG_778:g.145790A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000559133.6:c.1960+26A>G | ENSP00000453958.2:n.1960+26A>G | |
| ENST00000674301.2:c.1960+26A>G | ENSP00000501333.2:n.1960+26A>G | |
| ENST00000684448.1:n.634+26A>G | ||
| ENST00000316623.10:c.1960+26A>G MANE Select | ENSP00000325527.5:n.1960+26A>G | |
| ENST00000316623.9:c.1960+26A>G | ENSP00000325527.5:n.1960+26A>G | |
| ENST00000537463.6:c.637-30349A>G | ENSP00000440294.2:n.637-30349A>G | |
| NM_000138.4:c.1960+26A>G , LRG_778t1:c.1960+26A>G | NP_000129.3:n.1960+26A>G | |
| NM_000138.5:c.1960+26A>G MANE Select | NP_000129.3:n.1960+26A>G |