Linked Data
dbSNP Id:
rs2102951169
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171651989C>T , CM000663.2:g.171651989C>T | GRCh38 |
| NC_000001.10:g.171621129C>T , CM000663.1:g.171621129C>T | GRCh37 |
| NC_000001.9:g.169887752C>T | NCBI36 |
| NG_008859.1:g.5645G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.604+19G>A MANE Select | ENSP00000037502.5:n.604+19G>A | |
| ENST00000638471.1:c.130+493G>A | ENSP00000491206.1:n.130+493G>A | |
| ENST00000037502.10:c.604+19G>A | ENSP00000037502.5:n.604+19G>A | |
| ENST00000614688.1:c.604+19G>A | ENSP00000478680.1:n.604+19G>A | |
| NM_000261.1:c.604+19G>A | NP_000252.1:n.604+19G>A | |
| NM_000261.2:c.604+19G>A MANE Select | NP_000252.1:n.604+19G>A |